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Clinical research in general medical journals.

The New England journal of medicine

Boen JR.
PMID: 503144
N Engl J Med. 1979 Dec 06;301(23):1292. doi: 10.1056/NEJM197912063012321.

No abstract available.

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Boen JR. Clinical research in general medical journals. N Engl J Med. 1979;301(23):1292doi: 10.1056/NEJM197912063012321.
Boen, J. R. (1979). Clinical research in general medical journals. The New England journal of medicine, 301(23), 1292. https://doi.org/10.1056/NEJM197912063012321
Boen, J R. "Clinical research in general medical journals." The New England journal of medicine vol. 301,23 (1979): 1292. doi: https://doi.org/10.1056/NEJM197912063012321
Boen JR. Clinical research in general medical journals. N Engl J Med. 1979 Dec 06;301(23):1292. doi: 10.1056/NEJM197912063012321. PMID: 503144.
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Spinal Trauma and Symptoms in High School Football Players.

The Physician and sportsmedicine

Gerberich SG, Priest JD, Boen JR, Straub CP.
PMID: 27431967
Phys Sportsmed. 1983 Sep;11(9):122-40. doi: 10.1080/00913847.1983.11708641.

In brief: Responses from 101 coaches (98%) and 3,063 players (81%) In a retrospective epidemiological study of 103 Minnesota secondary school varsity football teams showed an overall injury rate of 78 injuries per 100 players, which included a high...

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Gerberich SG, Priest JD, Boen JR, et al. Spinal Trauma and Symptoms in High School Football Players. Phys Sportsmed. 1983;11(9):122-40doi: 10.1080/00913847.1983.11708641.
Gerberich, S. G., Priest, J. D., Boen, J. R., & Straub, C. P. (1983). Spinal Trauma and Symptoms in High School Football Players. The Physician and sportsmedicine, 11(9), 122-40. https://doi.org/10.1080/00913847.1983.11708641
Gerberich, S G, et al. "Spinal Trauma and Symptoms in High School Football Players." The Physician and sportsmedicine vol. 11,9 (1983): 122-40. doi: https://doi.org/10.1080/00913847.1983.11708641
Gerberich SG, Priest JD, Boen JR, Straub CP. Spinal Trauma and Symptoms in High School Football Players. Phys Sportsmed. 1983 Sep;11(9):122-40. doi: 10.1080/00913847.1983.11708641. PMID: 27431967.
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Joint analysis of BICEP2/keck array and Planck Data.

Physical review letters

Ade PA, Aghanim N, Ahmed Z, Aikin RW, Alexander KD, Arnaud M, Aumont J, Baccigalupi C, Banday AJ, Barkats D, Barreiro RB, Bartlett JG, Bartolo N, Battaner E, Benabed K, Benoît A, Benoit-Lévy A, Benton SJ, Bernard JP, Bersanelli M, Bielewicz P, Bischoff CA, Bock JJ, Bonaldi A, Bonavera L, Bond JR, Borrill J, Bouchet FR, Boulanger F, Brevik JA, Bucher M, Buder I, Bullock E, Burigana C, Butler RC, Buza V, Calabrese E, Cardoso JF, Catalano A, Challinor A, Chary RR, Chiang HC, Christensen PR, Colombo LP, Combet C, Connors J, Couchot F, Coulais A, Crill BP, Curto A, Cuttaia F, Danese L, Davies RD, Davis RJ, de Bernardis P, de Rosa A, de Zotti G, Delabrouille J, Delouis JM, Désert FX, Dickinson C, Diego JM, Dole H, Donzelli S, Doré O, Douspis M, Dowell CD, Duband L, Ducout A, Dunkley J, Dupac X, Dvorkin C, Efstathiou G, Elsner F, Enßlin TA, Eriksen HK, Falgarone E, Filippini JP, Finelli F, Fliescher S, Forni O, Frailis M, Fraisse AA, Franceschi E, Frejsel A, Galeotta S, Galli S, Ganga K, Ghosh T, Giard M, Gjerløw E, Golwala SR, González-Nuevo J, Górski KM, Gratton S, Gregorio A, Gruppuso A, Gudmundsson JE, Halpern M, Hansen FK, Hanson D, Harrison DL, Hasselfield M, Helou G, Henrot-Versillé S, Herranz D, Hildebrandt SR, Hilton GC, Hivon E, Hobson M, Holmes WA, Hovest W, Hristov VV, Huffenberger KM, Hui H, Hurier G, Irwin KD, Jaffe AH, Jaffe TR, Jewell J, Jones WC, Juvela M, Karakci A, Karkare KS, Kaufman JP, Keating BG, Kefeli S, Keihänen E, Kernasovskiy SA, Keskitalo R, Kisner TS, Kneissl R, Knoche J, Knox L, Kovac JM, Krachmalnicoff N, Kunz M, Kuo CL, Kurki-Suonio H, Lagache G, Lähteenmäki A, Lamarre JM, Lasenby A, Lattanzi M, Lawrence CR, Leitch EM, Leonardi R, Levrier F, Lewis A, Liguori M, Lilje PB, Linden-Vørnle M, López-Caniego M, Lubin PM, Lueker M, Macías-Pérez JF, Maffei B, Maino D, Mandolesi N, Mangilli A, Maris M, Martin PG, Martínez-González E, Masi S, Mason P, Matarrese S, Megerian KG, Meinhold PR, Melchiorri A, Mendes L, Mennella A, Migliaccio M, Mitra S, Miville-Deschênes MA, Moneti A, Montier L, Morgante G, Mortlock D, Moss A, Munshi D, Murphy JA, Naselsky P, Nati F, Natoli P, Netterfield CB, Nguyen HT, Nørgaard-Nielsen HU, Noviello F, Novikov D, Novikov I, O'Brient R, Ogburn RW, Orlando A, Pagano L, Pajot F, Paladini R, Paoletti D, Partridge B, Pasian F, Patanchon G, Pearson TJ, Perdereau O, Perotto L, Pettorino V, Piacentini F, Piat M, Pietrobon D, Plaszczynski S, Pointecouteau E, Polenta G, Ponthieu N, Pratt GW, Prunet S, Pryke C, Puget JL, Rachen JP, Reach WT, Rebolo R, Reinecke M, Remazeilles M, Renault C, Renzi A, Richter S, Ristorcelli I, Rocha G, Rossetti M, Roudier G, Rowan-Robinson M, Rubiño-Martín JA, Rusholme B, Sandri M, Santos D, Savelainen M, Savini G, Schwarz R, Scott D, Seiffert MD, Sheehy CD, Spencer LD, Staniszewski ZK, Stolyarov V, Sudiwala R, Sunyaev R, Sutton D, Suur-Uski AS, Sygnet JF, Tauber JA, Teply GP, Terenzi L, Thompson KL, Toffolatti L, Tolan JE, Tomasi M, Tristram M, Tucci M, Turner AD, Valenziano L, Valiviita J, Van Tent B, Vibert L, Vielva P, Vieregg AG, Villa F, Wade LA, Wandelt BD, Watson R, Weber AC, Wehus IK, White M, White SD, Willmert J, Wong CL, Yoon KW, Yvon D, Zacchei A, Zonca A.
PMID: 25815919
Phys Rev Lett. 2015 Mar 13;114(10):101301. doi: 10.1103/PhysRevLett.114.101301. Epub 2015 Mar 09.

We report the results of a joint analysis of data from BICEP2/Keck Array and Planck. BICEP2 and Keck Array have observed the same approximately 400  deg^{2} patch of sky centered on RA 0 h, Dec. -57.5°. The combined maps...

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Ade PA, Aghanim N, Ahmed Z, et al. Joint analysis of BICEP2/keck array and Planck Data. Phys Rev Lett. 2015;114(10):101301doi: 10.1103/PhysRevLett.114.101301.
Ade, P. A., Aghanim, N., Ahmed, Z., Aikin, R. W., Alexander, K. D., Arnaud, M., Aumont, J., Baccigalupi, C., Banday, A. J., Barkats, D., Barreiro, R. B., Bartlett, J. G., Bartolo, N., Battaner, E., Benabed, K., Benoît, A., Benoit-Lévy, A., Benton, S. J., Bernard, J. P., Bersanelli, M., Bielewicz, P., Bischoff, C. A., Bock, J. J., Bonaldi, A., Bonavera, L., Bond, J. R., Borrill, J., Bouchet, F. R., Boulanger, F., Brevik, J. A., Bucher, M., Buder, I., Bullock, E., Burigana, C., Butler, R. C., Buza, V., Calabrese, E., Cardoso, J. F., Catalano, A., Challinor, A., Chary, R. R., Chiang, H. C., Christensen, P. R., Colombo, L. P., Combet, C., Connors, J., Couchot, F., Coulais, A., Crill, B. P., Curto, A., Cuttaia, F., Danese, L., Davies, R. D., Davis, R. J., de Bernardis, P., de Rosa, A., de Zotti, G., Delabrouille, J., Delouis, J. M., Désert, F. X., Dickinson, C., Diego, J. M., Dole, H., Donzelli, S., Doré, O., Douspis, M., Dowell, C. D., Duband, L., Ducout, A., Dunkley, J., Dupac, X., Dvorkin, C., Efstathiou, G., Elsner, F., Enßlin, T. A., Eriksen, H. K., Falgarone, E., Filippini, J. P., Finelli, F., Fliescher, S., Forni, O., Frailis, M., Fraisse, A. A., Franceschi, E., Frejsel, A., Galeotta, S., Galli, S., Ganga, K., Ghosh, T., Giard, M., Gjerløw, E., Golwala, S. R., González-Nuevo, J., Górski, K. M., Gratton, S., Gregorio, A., Gruppuso, A., Gudmundsson, J. E., Halpern, M., Hansen, F. K., Hanson, D., Harrison, D. L., Hasselfield, M., Helou, G., Henrot-Versillé, S., Herranz, D., Hildebrandt, S. R., Hilton, G. C., Hivon, E., Hobson, M., Holmes, W. A., Hovest, W., Hristov, V. V., Huffenberger, K. M., Hui, H., Hurier, G., Irwin, K. D., Jaffe, A. H., Jaffe, T. R., Jewell, J., Jones, W. C., Juvela, M., Karakci, A., Karkare, K. S., Kaufman, J. P., Keating, B. G., Kefeli, S., Keihänen, E., Kernasovskiy, S. A., Keskitalo, R., Kisner, T. S., Kneissl, R., Knoche, J., Knox, L., Kovac, J. M., Krachmalnicoff, N., Kunz, M., Kuo, C. L., Kurki-Suonio, H., Lagache, G., Lähteenmäki, A., Lamarre, J. M., Lasenby, A., Lattanzi, M., Lawrence, C. R., Leitch, E. M., Leonardi, R., Levrier, F., Lewis, A., Liguori, M., Lilje, P. B., Linden-Vørnle, M., López-Caniego, M., Lubin, P. M., Lueker, M., Macías-Pérez, J. F., Maffei, B., Maino, D., Mandolesi, N., Mangilli, A., Maris, M., Martin, P. G., Martínez-González, E., Masi, S., Mason, P., Matarrese, S., Megerian, K. G., Meinhold, P. R., Melchiorri, A., Mendes, L., Mennella, A., Migliaccio, M., Mitra, S., Miville-Deschênes, M. A., Moneti, A., Montier, L., Morgante, G., Mortlock, D., Moss, A., Munshi, D., Murphy, J. A., Naselsky, P., Nati, F., Natoli, P., Netterfield, C. B., Nguyen, H. T., Nørgaard-Nielsen, H. U., Noviello, F., Novikov, D., Novikov, I., O'Brient, R., Ogburn, R. W., Orlando, A., Pagano, L., Pajot, F., Paladini, R., Paoletti, D., Partridge, B., Pasian, F., Patanchon, G., Pearson, T. J., Perdereau, O., Perotto, L., Pettorino, V., Piacentini, F., Piat, M., Pietrobon, D., Plaszczynski, S., Pointecouteau, E., Polenta, G., Ponthieu, N., Pratt, G. W., Prunet, S., Pryke, C., Puget, J. L., Rachen, J. P., Reach, W. T., Rebolo, R., Reinecke, M., Remazeilles, M., Renault, C., Renzi, A., Richter, S., Ristorcelli, I., Rocha, G., Rossetti, M., Roudier, G., Rowan-Robinson, M., Rubiño-Martín, J. A., Rusholme, B., Sandri, M., Santos, D., Savelainen, M., Savini, G., Schwarz, R., Scott, D., Seiffert, M. D., Sheehy, C. D., Spencer, L. D., Staniszewski, Z. K., Stolyarov, V., Sudiwala, R., Sunyaev, R., Sutton, D., Suur-Uski, A. S., Sygnet, J. F., Tauber, J. A., Teply, G. P., Terenzi, L., Thompson, K. L., Toffolatti, L., Tolan, J. E., Tomasi, M., Tristram, M., Tucci, M., Turner, A. D., Valenziano, L., Valiviita, J., Van Tent, B., Vibert, L., Vielva, P., Vieregg, A. G., Villa, F., Wade, L. A., Wandelt, B. D., Watson, R., Weber, A. C., Wehus, I. K., White, M., White, S. D., Willmert, J., Wong, C. L., Yoon, K. W., Yvon, D., Zacchei, A., Zonca, A. (2015). Joint analysis of BICEP2/keck array and Planck Data. Physical review letters, 114(10), 101301. https://doi.org/10.1103/PhysRevLett.114.101301
Ade, P A R, et al. "Joint analysis of BICEP2/keck array and Planck Data." Physical review letters vol. 114,10 (2015): 101301. doi: https://doi.org/10.1103/PhysRevLett.114.101301
Ade PA, Aghanim N, Ahmed Z, Aikin RW, Alexander KD, Arnaud M, Aumont J, Baccigalupi C, Banday AJ, Barkats D, Barreiro RB, Bartlett JG, Bartolo N, Battaner E, Benabed K, Benoît A, Benoit-Lévy A, Benton SJ, Bernard JP, Bersanelli M, Bielewicz P, Bischoff CA, Bock JJ, Bonaldi A, Bonavera L, Bond JR, Borrill J, Bouchet FR, Boulanger F, Brevik JA, Bucher M, Buder I, Bullock E, Burigana C, Butler RC, Buza V, Calabrese E, Cardoso JF, Catalano A, Challinor A, Chary RR, Chiang HC, Christensen PR, Colombo LP, Combet C, Connors J, Couchot F, Coulais A, Crill BP, Curto A, Cuttaia F, Danese L, Davies RD, Davis RJ, de Bernardis P, de Rosa A, de Zotti G, Delabrouille J, Delouis JM, Désert FX, Dickinson C, Diego JM, Dole H, Donzelli S, Doré O, Douspis M, Dowell CD, Duband L, Ducout A, Dunkley J, Dupac X, Dvorkin C, Efstathiou G, Elsner F, Enßlin TA, Eriksen HK, Falgarone E, Filippini JP, Finelli F, Fliescher S, Forni O, Frailis M, Fraisse AA, Franceschi E, Frejsel A, Galeotta S, Galli S, Ganga K, Ghosh T, Giard M, Gjerløw E, Golwala SR, González-Nuevo J, Górski KM, Gratton S, Gregorio A, Gruppuso A, Gudmundsson JE, Halpern M, Hansen FK, Hanson D, Harrison DL, Hasselfield M, Helou G, Henrot-Versillé S, Herranz D, Hildebrandt SR, Hilton GC, Hivon E, Hobson M, Holmes WA, Hovest W, Hristov VV, Huffenberger KM, Hui H, Hurier G, Irwin KD, Jaffe AH, Jaffe TR, Jewell J, Jones WC, Juvela M, Karakci A, Karkare KS, Kaufman JP, Keating BG, Kefeli S, Keihänen E, Kernasovskiy SA, Keskitalo R, Kisner TS, Kneissl R, Knoche J, Knox L, Kovac JM, Krachmalnicoff N, Kunz M, Kuo CL, Kurki-Suonio H, Lagache G, Lähteenmäki A, Lamarre JM, Lasenby A, Lattanzi M, Lawrence CR, Leitch EM, Leonardi R, Levrier F, Lewis A, Liguori M, Lilje PB, Linden-Vørnle M, López-Caniego M, Lubin PM, Lueker M, Macías-Pérez JF, Maffei B, Maino D, Mandolesi N, Mangilli A, Maris M, Martin PG, Martínez-González E, Masi S, Mason P, Matarrese S, Megerian KG, Meinhold PR, Melchiorri A, Mendes L, Mennella A, Migliaccio M, Mitra S, Miville-Deschênes MA, Moneti A, Montier L, Morgante G, Mortlock D, Moss A, Munshi D, Murphy JA, Naselsky P, Nati F, Natoli P, Netterfield CB, Nguyen HT, Nørgaard-Nielsen HU, Noviello F, Novikov D, Novikov I, O'Brient R, Ogburn RW, Orlando A, Pagano L, Pajot F, Paladini R, Paoletti D, Partridge B, Pasian F, Patanchon G, Pearson TJ, Perdereau O, Perotto L, Pettorino V, Piacentini F, Piat M, Pietrobon D, Plaszczynski S, Pointecouteau E, Polenta G, Ponthieu N, Pratt GW, Prunet S, Pryke C, Puget JL, Rachen JP, Reach WT, Rebolo R, Reinecke M, Remazeilles M, Renault C, Renzi A, Richter S, Ristorcelli I, Rocha G, Rossetti M, Roudier G, Rowan-Robinson M, Rubiño-Martín JA, Rusholme B, Sandri M, Santos D, Savelainen M, Savini G, Schwarz R, Scott D, Seiffert MD, Sheehy CD, Spencer LD, Staniszewski ZK, Stolyarov V, Sudiwala R, Sunyaev R, Sutton D, Suur-Uski AS, Sygnet JF, Tauber JA, Teply GP, Terenzi L, Thompson KL, Toffolatti L, Tolan JE, Tomasi M, Tristram M, Tucci M, Turner AD, Valenziano L, Valiviita J, Van Tent B, Vibert L, Vielva P, Vieregg AG, Villa F, Wade LA, Wandelt BD, Watson R, Weber AC, Wehus IK, White M, White SD, Willmert J, Wong CL, Yoon KW, Yvon D, Zacchei A, Zonca A. Joint analysis of BICEP2/keck array and Planck Data. Phys Rev Lett. 2015 Mar 13;114(10):101301. doi: 10.1103/PhysRevLett.114.101301. Epub 2015 Mar 09. PMID: 25815919.
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Evaluating more naturalistic outcome measures: A 1-year smartphone study in multiple sclerosis.

Neurology(R) neuroimmunology & neuroinflammation

Bove R, White CC, Giovannoni G, Glanz B, Golubchikov V, Hujol J, Jennings C, Langdon D, Lee M, Legedza A, Paskavitz J, Prasad S, Richert J, Robbins A, Roberts S, Weiner H, Ramachandran R, Botfield M, De Jager PL.
PMID: 26516627
Neurol Neuroimmunol Neuroinflamm. 2015 Oct 15;2(6):e162. doi: 10.1212/NXI.0000000000000162. eCollection 2015 Dec.

OBJECTIVE: In this cohort of individuals with and without multiple sclerosis (MS), we illustrate some of the novel approaches that smartphones provide to monitor patients with chronic neurologic disorders in their natural setting.METHODS: Thirty-eight participant pairs (MS and cohabitant)...

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Bove R, White CC, Giovannoni G, et al. Evaluating more naturalistic outcome measures: A 1-year smartphone study in multiple sclerosis. Neurol Neuroimmunol Neuroinflamm. 2015;2(6):e162doi: 10.1212/NXI.0000000000000162.
Bove, R., White, C. C., Giovannoni, G., Glanz, B., Golubchikov, V., Hujol, J., Jennings, C., Langdon, D., Lee, M., Legedza, A., Paskavitz, J., Prasad, S., Richert, J., Robbins, A., Roberts, S., Weiner, H., Ramachandran, R., Botfield, M., & De Jager, P. L. (2015). Evaluating more naturalistic outcome measures: A 1-year smartphone study in multiple sclerosis. Neurology(R) neuroimmunology & neuroinflammation, 2(6), e162. https://doi.org/10.1212/NXI.0000000000000162
Bove, Riley, et al. "Evaluating more naturalistic outcome measures: A 1-year smartphone study in multiple sclerosis." Neurology(R) neuroimmunology & neuroinflammation vol. 2,6 (2015): e162. doi: https://doi.org/10.1212/NXI.0000000000000162
Bove R, White CC, Giovannoni G, Glanz B, Golubchikov V, Hujol J, Jennings C, Langdon D, Lee M, Legedza A, Paskavitz J, Prasad S, Richert J, Robbins A, Roberts S, Weiner H, Ramachandran R, Botfield M, De Jager PL. Evaluating more naturalistic outcome measures: A 1-year smartphone study in multiple sclerosis. Neurol Neuroimmunol Neuroinflamm. 2015 Oct 15;2(6):e162. doi: 10.1212/NXI.0000000000000162. eCollection 2015 Dec. PMID: 26516627; PMCID: PMC4608760.
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Aldehydic contact poisons and alarm pheromone of the antCrematogaster scutellaris (Hymenoptera: Myrmicinae) : Enzyme-Mediated Production from acetate precursors.

Journal of chemical ecology

Pasteels JM, Daloze D, Boeve JL.
PMID: 24272094
J Chem Ecol. 1989 May;15(5):1501-11. doi: 10.1007/BF01012379.

The Dufour gland ofCrematogaster scutellaris stores a mixture of long-chain primary acetates bearing a cross-conjugated dienone (Scheme 1, la-c). The poison gland contains two highly active enzymes: an acetate esterase and an alcohol oxidase. During venom emission, the constituents...

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Pasteels JM, Daloze D, Boeve JL. Aldehydic contact poisons and alarm pheromone of the antCrematogaster scutellaris (Hymenoptera: Myrmicinae) : Enzyme-Mediated Production from acetate precursors. J Chem Ecol. 1989;15(5):1501-11doi: 10.1007/BF01012379.
Pasteels, J. M., Daloze, D., & Boeve, J. L. (1989). Aldehydic contact poisons and alarm pheromone of the antCrematogaster scutellaris (Hymenoptera: Myrmicinae) : Enzyme-Mediated Production from acetate precursors. Journal of chemical ecology, 15(5), 1501-11. https://doi.org/10.1007/BF01012379
Pasteels, J M, et al. "Aldehydic contact poisons and alarm pheromone of the antCrematogaster scutellaris (Hymenoptera: Myrmicinae) : Enzyme-Mediated Production from acetate precursors." Journal of chemical ecology vol. 15,5 (1989): 1501-11. doi: https://doi.org/10.1007/BF01012379
Pasteels JM, Daloze D, Boeve JL. Aldehydic contact poisons and alarm pheromone of the antCrematogaster scutellaris (Hymenoptera: Myrmicinae) : Enzyme-Mediated Production from acetate precursors. J Chem Ecol. 1989 May;15(5):1501-11. doi: 10.1007/BF01012379. PMID: 24272094.
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The relationship between socioeconomic variables and major mental illness in the counties of a midwestern state.

Community mental health journal

Vail DJ, Lucero RJ, Boen JR.
PMID: 24190817
Community Ment Health J. 1966 Sep;2(3):211-2. doi: 10.1007/BF01419682.

A total of 77 socioeconomic and demographic variables and 46 indices of bio-psycho-social dysfunction were gathered on each of Minnesota's 87 counties. All of these were expressed in rates per 10,000 population or other standard figures. Various analyses were...

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Vail DJ, Lucero RJ, Boen JR. The relationship between socioeconomic variables and major mental illness in the counties of a midwestern state. Community Ment Health J. 1966;2(3):211-2doi: 10.1007/BF01419682.
Vail, D. J., Lucero, R. J., & Boen, J. R. (1966). The relationship between socioeconomic variables and major mental illness in the counties of a midwestern state. Community mental health journal, 2(3), 211-2. https://doi.org/10.1007/BF01419682
Vail, D J, et al. "The relationship between socioeconomic variables and major mental illness in the counties of a midwestern state." Community mental health journal vol. 2,3 (1966): 211-2. doi: https://doi.org/10.1007/BF01419682
Vail DJ, Lucero RJ, Boen JR. The relationship between socioeconomic variables and major mental illness in the counties of a midwestern state. Community Ment Health J. 1966 Sep;2(3):211-2. doi: 10.1007/BF01419682. PMID: 24190817.
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Synthesis of chemically and configurationally stable monofluoro acylboronates: effect of ligand structure on their formation, properties, and reactivities.

Journal of the American Chemical Society

Noda H, Bode JW.
PMID: 25723308
J Am Chem Soc. 2015 Mar 25;137(11):3958-66. doi: 10.1021/jacs.5b00822. Epub 2015 Mar 13.

The recent disclosures of two classes of acylborons, potassium acyltrifluoroborates (KATs) and N-methyliminodiacetyl (MIDA) acylboronates, demonstrated that certain acylboron species can be both remarkably stable and uniquely reactive. Here we report new classes of ligands for acylboronates that have...

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Noda H, Bode JW. Synthesis of chemically and configurationally stable monofluoro acylboronates: effect of ligand structure on their formation, properties, and reactivities. J Am Chem Soc. 2015;137(11):3958-66doi: 10.1021/jacs.5b00822.
Noda, H., & Bode, J. W. (2015). Synthesis of chemically and configurationally stable monofluoro acylboronates: effect of ligand structure on their formation, properties, and reactivities. Journal of the American Chemical Society, 137(11), 3958-66. https://doi.org/10.1021/jacs.5b00822
Noda, Hidetoshi, and Bode, Jeffrey W. "Synthesis of chemically and configurationally stable monofluoro acylboronates: effect of ligand structure on their formation, properties, and reactivities." Journal of the American Chemical Society vol. 137,11 (2015): 3958-66. doi: https://doi.org/10.1021/jacs.5b00822
Noda H, Bode JW. Synthesis of chemically and configurationally stable monofluoro acylboronates: effect of ligand structure on their formation, properties, and reactivities. J Am Chem Soc. 2015 Mar 25;137(11):3958-66. doi: 10.1021/jacs.5b00822. Epub 2015 Mar 13. PMID: 25723308.
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Synthesis of Bifunctional Potassium Acyltrifluoroborates.

Organic letters

Liu SM, Mazunin D, Pattabiraman VR, Bode JW.
PMID: 27709962
Org Lett. 2016 Oct 21;18(20):5336-5339. doi: 10.1021/acs.orglett.6b02652. Epub 2016 Oct 06.

New bifunctional potassium acyltrifluoroborate (KAT) substrates have been synthesized in gram scale using optimized reaction conditions. Chemoselective transformation of functional groups in the presence of an acyltrifluoroborate has been demonstrated, and orthogonal reactions of bifunctional KAT reagents are reported....

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Liu SM, Mazunin D, Pattabiraman VR, et al. Synthesis of Bifunctional Potassium Acyltrifluoroborates. Org Lett. 2016;18(20):5336-5339doi: 10.1021/acs.orglett.6b02652.
Liu, S. M., Mazunin, D., Pattabiraman, V. R., & Bode, J. W. (2016). Synthesis of Bifunctional Potassium Acyltrifluoroborates. Organic letters, 18(20), 5336-5339. https://doi.org/10.1021/acs.orglett.6b02652
Liu, Sizhou M, et al. "Synthesis of Bifunctional Potassium Acyltrifluoroborates." Organic letters vol. 18,20 (2016): 5336-5339. doi: https://doi.org/10.1021/acs.orglett.6b02652
Liu SM, Mazunin D, Pattabiraman VR, Bode JW. Synthesis of Bifunctional Potassium Acyltrifluoroborates. Org Lett. 2016 Oct 21;18(20):5336-5339. doi: 10.1021/acs.orglett.6b02652. Epub 2016 Oct 06. PMID: 27709962.
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Oriented migration of interstitial cells and nematocytes inHydra attenuata.

Wilhelm Roux' Archiv fur Entwicklungsmechanik der Organismen

Herlands RL, Bode HR.
PMID: 28304816
Wilhelm Roux Arch Entwickl Mech Org. 1974 Mar;176(1):67-88. doi: 10.1007/BF00577831.

The migratory properties of hydra cells within the tissue were studied. The extent and direction of cell migration were examined in budding, non-budding, and regenerating animals. Nematocytes and a small number of single big interstitial cells (the multipotent interstitial...

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Herlands RL, Bode HR. Oriented migration of interstitial cells and nematocytes inHydra attenuata. Wilhelm Roux Arch Entwickl Mech Org. 1974;176(1):67-88doi: 10.1007/BF00577831.
Herlands, R. L., & Bode, H. R. (1974). Oriented migration of interstitial cells and nematocytes inHydra attenuata. Wilhelm Roux' Archiv fur Entwicklungsmechanik der Organismen, 176(1), 67-88. https://doi.org/10.1007/BF00577831
Herlands, Rosalind L, and Bode, Hans R. "Oriented migration of interstitial cells and nematocytes inHydra attenuata." Wilhelm Roux' Archiv fur Entwicklungsmechanik der Organismen vol. 176,1 (1974): 67-88. doi: https://doi.org/10.1007/BF00577831
Herlands RL, Bode HR. Oriented migration of interstitial cells and nematocytes inHydra attenuata. Wilhelm Roux Arch Entwickl Mech Org. 1974 Mar;176(1):67-88. doi: 10.1007/BF00577831. PMID: 28304816.
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Spatial and temporal use of floodplain habitats by lentic and lotic species of aquatic turtles.

Oecologia

Bodie JR, Semlitsch RD.
PMID: 28307951
Oecologia. 2000 Jan;122(1):138-146. doi: 10.1007/PL00008830.

We investigated the use of aquatic and terrestrial floodplain habitats by lentic and lotic turtles inhabiting the Missouri River, a contemporary, regulated large river. Specifically, we tested whether habitats were used differentially by turtle species, sexes, and life stages...

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Bodie JR, Semlitsch RD. Spatial and temporal use of floodplain habitats by lentic and lotic species of aquatic turtles. Oecologia. 2000;122(1):138-146doi: 10.1007/PL00008830.
Bodie, J. R., & Semlitsch, R. D. (2000). Spatial and temporal use of floodplain habitats by lentic and lotic species of aquatic turtles. Oecologia, 122(1), 138-146. https://doi.org/10.1007/PL00008830
Bodie, J R, and Semlitsch, R D. "Spatial and temporal use of floodplain habitats by lentic and lotic species of aquatic turtles." Oecologia vol. 122,1 (2000): 138-146. doi: https://doi.org/10.1007/PL00008830
Bodie JR, Semlitsch RD. Spatial and temporal use of floodplain habitats by lentic and lotic species of aquatic turtles. Oecologia. 2000 Jan;122(1):138-146. doi: 10.1007/PL00008830. PMID: 28307951.
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Synthesis of Acylborons by Ozonolysis of Alkenylboronates: Preparation of an Enantioenriched Amino Acid Acylboronate.

Angewandte Chemie (International ed. in English)

Taguchi J, Ikeda T, Takahashi R, Sasaki I, Ogasawara Y, Dairi T, Kato N, Yamamoto Y, Bode JW, Ito H.
PMID: 28905460
Angew Chem Int Ed Engl. 2017 Oct 23;56(44):13847-13851. doi: 10.1002/anie.201707933. Epub 2017 Sep 29.

A concise synthesis of acylborons was achieved by ozonolysis of alkenyl MIDA (N-methyliminodiacetic acid) boronates. This reaction exhibits excellent functional-group tolerance and is applicable to various acyl MIDA boronates and potassium acyltrifluroborates (KATs) which could not be synthesized by...

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Taguchi J, Ikeda T, Takahashi R, et al. Synthesis of Acylborons by Ozonolysis of Alkenylboronates: Preparation of an Enantioenriched Amino Acid Acylboronate. Angew Chem Int Ed Engl. 2017;56(44):13847-13851doi: 10.1002/anie.201707933.
Taguchi, J., Ikeda, T., Takahashi, R., Sasaki, I., Ogasawara, Y., Dairi, T., Kato, N., Yamamoto, Y., Bode, J. W., & Ito, H. (2017). Synthesis of Acylborons by Ozonolysis of Alkenylboronates: Preparation of an Enantioenriched Amino Acid Acylboronate. Angewandte Chemie (International ed. in English), 56(44), 13847-13851. https://doi.org/10.1002/anie.201707933
Taguchi, Jumpei, et al. "Synthesis of Acylborons by Ozonolysis of Alkenylboronates: Preparation of an Enantioenriched Amino Acid Acylboronate." Angewandte Chemie (International ed. in English) vol. 56,44 (2017): 13847-13851. doi: https://doi.org/10.1002/anie.201707933
Taguchi J, Ikeda T, Takahashi R, Sasaki I, Ogasawara Y, Dairi T, Kato N, Yamamoto Y, Bode JW, Ito H. Synthesis of Acylborons by Ozonolysis of Alkenylboronates: Preparation of an Enantioenriched Amino Acid Acylboronate. Angew Chem Int Ed Engl. 2017 Oct 23;56(44):13847-13851. doi: 10.1002/anie.201707933. Epub 2017 Sep 29. PMID: 28905460.
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A novel, general method for the synthesis of nitrile oxides: dehydration of O-silylated hydroxamic acids.

Organic letters

Muri D, Bode JW, Carreira EM.
PMID: 10814371
Org Lett. 2000 Feb 24;2(4):539-41. doi: 10.1021/ol991396q.

[reaction: see text] O-Silylated hydroxamic acids serve as stable, readily accessible, crystalline precursors to nitrile oxides when treated with trifluoromethanesulfonic anhydride and triethylamine. Under these mild conditions in the presence of olefins O-silylated hydroxamic acids afford isoxazoline cycloadducts. This...

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Muri D, Bode JW, Carreira EM. A novel, general method for the synthesis of nitrile oxides: dehydration of O-silylated hydroxamic acids. Org Lett. 2000;2(4):539-41doi: 10.1021/ol991396q.
Muri, D., Bode, J. W., & Carreira, E. M. (2000). A novel, general method for the synthesis of nitrile oxides: dehydration of O-silylated hydroxamic acids. Organic letters, 2(4), 539-41. https://doi.org/10.1021/ol991396q
Muri, et al. "A novel, general method for the synthesis of nitrile oxides: dehydration of O-silylated hydroxamic acids." Organic letters vol. 2,4 (2000): 539-41. doi: https://doi.org/10.1021/ol991396q
Muri D, Bode JW, Carreira EM. A novel, general method for the synthesis of nitrile oxides: dehydration of O-silylated hydroxamic acids. Org Lett. 2000 Feb 24;2(4):539-41. doi: 10.1021/ol991396q. PMID: 10814371.
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