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Vibrational circular dichroism of 3-(trifluoroacetyl)-camphor and its interaction with chiral amines.

Chirality

Merten C, Jalkanen KJ, Weiss VC, Hartwig A.
PMID: 20186758
Chirality. 2010 Aug;22(8):772-7. doi: 10.1002/chir.20832.

Vibrational circular dichroism (VCD) spectroscopy and density functional theory (DFT) calculations are used to investigate the keto-enol equilibrium of 3-(trifluoroacetyl)-camphor (TFC) and to study the interaction of TFC with chiral amines in deuterated Chloroform. It is shown that the...

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Merten C, Jalkanen KJ, Weiss VC, et al. Vibrational circular dichroism of 3-(trifluoroacetyl)-camphor and its interaction with chiral amines. Chirality. 2010;22(8):772-7doi: 10.1002/chir.20832.
Merten, C., Jalkanen, K. J., Weiss, V. C., & Hartwig, A. (2010). Vibrational circular dichroism of 3-(trifluoroacetyl)-camphor and its interaction with chiral amines. Chirality, 22(8), 772-7. https://doi.org/10.1002/chir.20832
Merten, Christian, et al. "Vibrational circular dichroism of 3-(trifluoroacetyl)-camphor and its interaction with chiral amines." Chirality vol. 22,8 (2010): 772-7. doi: https://doi.org/10.1002/chir.20832
Merten C, Jalkanen KJ, Weiss VC, Hartwig A. Vibrational circular dichroism of 3-(trifluoroacetyl)-camphor and its interaction with chiral amines. Chirality. 2010 Aug;22(8):772-7. doi: 10.1002/chir.20832. PMID: 20186758.
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Linear-selective hydroarylation of unactivated terminal and internal olefins with trifluoromethyl-substituted arenes.

Journal of the American Chemical Society

Bair JS, Schramm Y, Sergeev AG, Clot E, Eisenstein O, Hartwig JF.
PMID: 25171744
J Am Chem Soc. 2014 Sep 24;136(38):13098-101. doi: 10.1021/ja505579f. Epub 2014 Sep 15.

We report a series of hydroarylations of unactivated olefins with trifluoromethyl-substituted arenes that occur with high selectivity for the linear product without directing groups on the arene. We also show that hydroarylations occur with internal, acyclic olefins to yield...

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Bair JS, Schramm Y, Sergeev AG, et al. Linear-selective hydroarylation of unactivated terminal and internal olefins with trifluoromethyl-substituted arenes. J Am Chem Soc. 2014;136(38):13098-101doi: 10.1021/ja505579f.
Bair, J. S., Schramm, Y., Sergeev, A. G., Clot, E., Eisenstein, O., & Hartwig, J. F. (2014). Linear-selective hydroarylation of unactivated terminal and internal olefins with trifluoromethyl-substituted arenes. Journal of the American Chemical Society, 136(38), 13098-101. https://doi.org/10.1021/ja505579f
Bair, Joseph S, et al. "Linear-selective hydroarylation of unactivated terminal and internal olefins with trifluoromethyl-substituted arenes." Journal of the American Chemical Society vol. 136,38 (2014): 13098-101. doi: https://doi.org/10.1021/ja505579f
Bair JS, Schramm Y, Sergeev AG, Clot E, Eisenstein O, Hartwig JF. Linear-selective hydroarylation of unactivated terminal and internal olefins with trifluoromethyl-substituted arenes. J Am Chem Soc. 2014 Sep 24;136(38):13098-101. doi: 10.1021/ja505579f. Epub 2014 Sep 15. PMID: 25171744.
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Correction: Kicking against the PRCs--A Domesticated Transposase Antagonises Silencing Mediated by Polycomb Group Proteins and Is an Accessory Component of Polycomb Repressive Complex 2.

PLoS genetics

Liang SC, Hartwig B, Perera P, Mora-García S, de Leau E, Thornton H, de Lima Alves F, Rappsilber J, Yang S, James GV, Schneeberger K, Finnegan EJ, Turck F, Goodrich J.
PMID: 26895156
PLoS Genet. 2016 Feb 19;12(2):e1005812. doi: 10.1371/journal.pgen.1005812. eCollection 2016 Feb.

No abstract available.

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Liang SC, Hartwig B, Perera P, et al. Correction: Kicking against the PRCs--A Domesticated Transposase Antagonises Silencing Mediated by Polycomb Group Proteins and Is an Accessory Component of Polycomb Repressive Complex 2. PLoS Genet. 2016;12(2):e1005812doi: 10.1371/journal.pgen.1005812.
Liang, S. C., Hartwig, B., Perera, P., Mora-García, S., de Leau, E., Thornton, H., de Lima Alves, F., Rappsilber, J., Yang, S., James, G. V., Schneeberger, K., Finnegan, E. J., Turck, F., & Goodrich, J. (2016). Correction: Kicking against the PRCs--A Domesticated Transposase Antagonises Silencing Mediated by Polycomb Group Proteins and Is an Accessory Component of Polycomb Repressive Complex 2. PLoS genetics, 12(2), e1005812. https://doi.org/10.1371/journal.pgen.1005812
Liang, Shih Chieh, et al. "Correction: Kicking against the PRCs--A Domesticated Transposase Antagonises Silencing Mediated by Polycomb Group Proteins and Is an Accessory Component of Polycomb Repressive Complex 2." PLoS genetics vol. 12,2 (2016): e1005812. doi: https://doi.org/10.1371/journal.pgen.1005812
Liang SC, Hartwig B, Perera P, Mora-García S, de Leau E, Thornton H, de Lima Alves F, Rappsilber J, Yang S, James GV, Schneeberger K, Finnegan EJ, Turck F, Goodrich J. Correction: Kicking against the PRCs--A Domesticated Transposase Antagonises Silencing Mediated by Polycomb Group Proteins and Is an Accessory Component of Polycomb Repressive Complex 2. PLoS Genet. 2016 Feb 19;12(2):e1005812. doi: 10.1371/journal.pgen.1005812. eCollection 2016 Feb. PMID: 26895156; PMCID: PMC4760731.
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Adsorption mechanism and valency of catechol-functionalized hyperbranched polyglycerols.

Beilstein journal of organic chemistry

Krysiak S, Wei Q, Rischka K, Hartwig A, Haag R, Hugel T.
PMID: 26150898
Beilstein J Org Chem. 2015 May 18;11:828-36. doi: 10.3762/bjoc.11.92. eCollection 2015.

Nature often serves as a model system for developing new adhesives. In aqueous environments, mussel-inspired adhesives are promising candidates. Understanding the mechanism of the extraordinarily strong adhesive bonds of the catechol group will likely aid in the development of...

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Krysiak S, Wei Q, Rischka K, et al. Adsorption mechanism and valency of catechol-functionalized hyperbranched polyglycerols. Beilstein J Org Chem. 2015;11:828-36doi: 10.3762/bjoc.11.92.
Krysiak, S., Wei, Q., Rischka, K., Hartwig, A., Haag, R., & Hugel, T. (2015). Adsorption mechanism and valency of catechol-functionalized hyperbranched polyglycerols. Beilstein journal of organic chemistry, 11828-36. https://doi.org/10.3762/bjoc.11.92
Krysiak, Stefanie, et al. "Adsorption mechanism and valency of catechol-functionalized hyperbranched polyglycerols." Beilstein journal of organic chemistry vol. 11 (2015): 828-36. doi: https://doi.org/10.3762/bjoc.11.92
Krysiak S, Wei Q, Rischka K, Hartwig A, Haag R, Hugel T. Adsorption mechanism and valency of catechol-functionalized hyperbranched polyglycerols. Beilstein J Org Chem. 2015 May 18;11:828-36. doi: 10.3762/bjoc.11.92. eCollection 2015. PMID: 26150898; PMCID: PMC4463490.
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Lung transplantation at Duke.

Journal of thoracic disease

Gray AL, Mulvihill MS, Hartwig MG.
PMID: 27076968
J Thorac Dis. 2016 Mar;8(3):E185-96. doi: 10.21037/jtd.2016.02.08.

Lung transplantation represents the gold-standard therapy for patients with end-stage lung disease. Utilization of this therapy continues to rise. The Lung Transplant Program at Duke University Medical Center was established in 1992, and since that time has grown to...

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Gray AL, Mulvihill MS, Hartwig MG. Lung transplantation at Duke. J Thorac Dis. 2016;8(3):E185-96doi: 10.21037/jtd.2016.02.08.
Gray, A. L., Mulvihill, M. S., & Hartwig, M. G. (2016). Lung transplantation at Duke. Journal of thoracic disease, 8(3), E185-96. https://doi.org/10.21037/jtd.2016.02.08
Gray, Alice L, et al. "Lung transplantation at Duke." Journal of thoracic disease vol. 8,3 (2016): E185-96. doi: https://doi.org/10.21037/jtd.2016.02.08
Gray AL, Mulvihill MS, Hartwig MG. Lung transplantation at Duke. J Thorac Dis. 2016 Mar;8(3):E185-96. doi: 10.21037/jtd.2016.02.08. PMID: 27076968; PMCID: PMC4805837.
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Chemoselective, Enzymatic C-H Bond Amination Catalyzed by a Cytochrome P450 Containing an Ir(Me)-PIX Cofactor.

Journal of the American Chemical Society

Dydio P, Key HM, Hayashi H, Clark DS, Hartwig JF.
PMID: 28080030
J Am Chem Soc. 2017 Feb 08;139(5):1750-1753. doi: 10.1021/jacs.6b11410. Epub 2017 Jan 26.

Cytochrome P450 enzymes have been engineered to catalyze abiological C-H bond amination reactions, but the yields of these reactions have been limited by low chemoselectivity for the amination of C-H bonds over competing reduction of the azide substrate to...

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Dydio P, Key HM, Hayashi H, et al. Chemoselective, Enzymatic C-H Bond Amination Catalyzed by a Cytochrome P450 Containing an Ir(Me)-PIX Cofactor. J Am Chem Soc. 2017;139(5):1750-1753doi: 10.1021/jacs.6b11410.
Dydio, P., Key, H. M., Hayashi, H., Clark, D. S., & Hartwig, J. F. (2017). Chemoselective, Enzymatic C-H Bond Amination Catalyzed by a Cytochrome P450 Containing an Ir(Me)-PIX Cofactor. Journal of the American Chemical Society, 139(5), 1750-1753. https://doi.org/10.1021/jacs.6b11410
Dydio, Paweł, et al. "Chemoselective, Enzymatic C-H Bond Amination Catalyzed by a Cytochrome P450 Containing an Ir(Me)-PIX Cofactor." Journal of the American Chemical Society vol. 139,5 (2017): 1750-1753. doi: https://doi.org/10.1021/jacs.6b11410
Dydio P, Key HM, Hayashi H, Clark DS, Hartwig JF. Chemoselective, Enzymatic C-H Bond Amination Catalyzed by a Cytochrome P450 Containing an Ir(Me)-PIX Cofactor. J Am Chem Soc. 2017 Feb 08;139(5):1750-1753. doi: 10.1021/jacs.6b11410. Epub 2017 Jan 26. PMID: 28080030.
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Feasibility of halogen determination in noncombustible inorganic matrices by ion chromatography after a novel volatilization method using microwave-induced combustion.

Talanta

Pereira RM, Costa VC, Hartwig CA, Picoloto RS, Flores EM, Duarte FA, Mesko MF.
PMID: 26592579
Talanta. 2016 Jan 15;147:76-81. doi: 10.1016/j.talanta.2015.09.031. Epub 2015 Sep 13.

A microwave-induced combustion (MIC) system based on the volatilization process was applied for subsequent halogen determination from noncombustible inorganic matrices. Portland cement samples were selected to demonstrate the feasibility of the proposed method, allowing the subsequent determination of Cl...

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Pereira RM, Costa VC, Hartwig CA, et al. Feasibility of halogen determination in noncombustible inorganic matrices by ion chromatography after a novel volatilization method using microwave-induced combustion. Talanta. 2015;147:76-81doi: 10.1016/j.talanta.2015.09.031.
Pereira, R. M., Costa, V. C., Hartwig, C. A., Picoloto, R. S., Flores, E. M., Duarte, F. A., & Mesko, M. F. (2016). Feasibility of halogen determination in noncombustible inorganic matrices by ion chromatography after a novel volatilization method using microwave-induced combustion. Talanta, 14776-81. https://doi.org/10.1016/j.talanta.2015.09.031
Pereira, Rodrigo M, et al. "Feasibility of halogen determination in noncombustible inorganic matrices by ion chromatography after a novel volatilization method using microwave-induced combustion." Talanta vol. 147 (2016): 76-81. doi: https://doi.org/10.1016/j.talanta.2015.09.031
Pereira RM, Costa VC, Hartwig CA, Picoloto RS, Flores EM, Duarte FA, Mesko MF. Feasibility of halogen determination in noncombustible inorganic matrices by ion chromatography after a novel volatilization method using microwave-induced combustion. Talanta. 2016 Jan 15;147:76-81. doi: 10.1016/j.talanta.2015.09.031. Epub 2015 Sep 13. PMID: 26592579.
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Patents and literature.

Applied biochemistry and biotechnology

Smith JA, Luenser SJ, Olson NF, Magee EL, Olivieri R, Viglia A, Degen L, Angelini L, Fascetti E, Miwa N, Masuda Y, Kawarabuki S, Sai T, Saito T, Busby MG, Hartwig DW, Heady R, Yagi Y, Kouno K, Inui T, Marshall JJ, Thomson AR, Miles BJ, Caygill JC, Moore DJ, Nakamura K, Nankai S, Iijima T, Ooshima Y, Baldeschwieler JD, Gamble RC, Mauk MR, Shen TY, Ponpipom MM, Khachatourians GG, Zaffaroni P, Senni A, Formiconi L, Blair JE, Davis LT, Cabane B, Vergnault J, Volesky B, Tsezos M, Bull FG, Messing RA, Ahnell JE, Chen LF, Gong CS, Tsao GT, Katsumata R, Green S, Leiser RS, Fedde PA, Ghosh S, Henry MP, Klass DL, Uemura Y, Arimura H, Morise H, Funakoshi S, Suyama T, Lützen NW, Kita DA, Fenton DM, Maclennan DG, Ousby JC, Owen TR, Steer DC, Araujo FJ, Calderon IL, Diaz IL, Olmedo C, Rebeller M, Yout P, Lonchamp D, Mynatt RL, Berg A, Eckmayer Z, Maselli JA, Horwath RO, Gotou E, Satou K, Wu RJ, Bahl CP, Narang SA, Hershberger CL, Baxter JD, Roberts JL, Seeburg PH, Goodman HM, Tsuchida T.
PMID: 24234462
Appl Biochem Biotechnol. 1982 Nov;7(6):497-510. doi: 10.1007/BF02799180.

No abstract available.

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Smith JA, Luenser SJ, Olson NF, et al. Patents and literature. Appl Biochem Biotechnol. 1982;7(6):497-510doi: 10.1007/BF02799180.
Smith, J. A., Luenser, S. J., Olson, N. F., Magee, E. L., Olivieri, R., Viglia, A., Degen, L., Angelini, L., Fascetti, E., Miwa, N., Masuda, Y., Kawarabuki, S., Sai, T., Saito, T., Busby, M. G., Hartwig, D. W., Heady, R., Yagi, Y., Kouno, K., Inui, T., Marshall, J. J., Thomson, A. R., Miles, B. J., Caygill, J. C., Moore, D. J., Nakamura, K., Nankai, S., Iijima, T., Ooshima, Y., Baldeschwieler, J. D., Gamble, R. C., Mauk, M. R., Shen, T. Y., Ponpipom, M. M., Khachatourians, G. G., Zaffaroni, P., Senni, A., Formiconi, L., Blair, J. E., Davis, L. T., Cabane, B., Vergnault, J., Volesky, B., Tsezos, M., Bull, F. G., Messing, R. A., Ahnell, J. E., Chen, L. F., Gong, C. S., Tsao, G. T., Katsumata, R., Green, S., Leiser, R. S., Fedde, P. A., Ghosh, S., Henry, M. P., Klass, D. L., Uemura, Y., Arimura, H., Morise, H., Funakoshi, S., Suyama, T., Lützen, N. W., Kita, D. A., Fenton, D. M., Maclennan, D. G., Ousby, J. C., Owen, T. R., Steer, D. C., Araujo, F. J., Calderon, I. L., Diaz, I. L., Olmedo, C., Rebeller, M., Yout, P., Lonchamp, D., Mynatt, R. L., Berg, A., Eckmayer, Z., Maselli, J. A., Horwath, R. O., Gotou, E., Satou, K., Wu, R. J., Bahl, C. P., Narang, S. A., Hershberger, C. L., Baxter, J. D., Roberts, J. L., Seeburg, P. H., Goodman, H. M., & Tsuchida, T. (1982). Patents and literature. Applied biochemistry and biotechnology, 7(6), 497-510. https://doi.org/10.1007/BF02799180
Smith, J A, et al. "Patents and literature." Applied biochemistry and biotechnology vol. 7,6 (1982): 497-510. doi: https://doi.org/10.1007/BF02799180
Smith JA, Luenser SJ, Olson NF, Magee EL, Olivieri R, Viglia A, Degen L, Angelini L, Fascetti E, Miwa N, Masuda Y, Kawarabuki S, Sai T, Saito T, Busby MG, Hartwig DW, Heady R, Yagi Y, Kouno K, Inui T, Marshall JJ, Thomson AR, Miles BJ, Caygill JC, Moore DJ, Nakamura K, Nankai S, Iijima T, Ooshima Y, Baldeschwieler JD, Gamble RC, Mauk MR, Shen TY, Ponpipom MM, Khachatourians GG, Zaffaroni P, Senni A, Formiconi L, Blair JE, Davis LT, Cabane B, Vergnault J, Volesky B, Tsezos M, Bull FG, Messing RA, Ahnell JE, Chen LF, Gong CS, Tsao GT, Katsumata R, Green S, Leiser RS, Fedde PA, Ghosh S, Henry MP, Klass DL, Uemura Y, Arimura H, Morise H, Funakoshi S, Suyama T, Lützen NW, Kita DA, Fenton DM, Maclennan DG, Ousby JC, Owen TR, Steer DC, Araujo FJ, Calderon IL, Diaz IL, Olmedo C, Rebeller M, Yout P, Lonchamp D, Mynatt RL, Berg A, Eckmayer Z, Maselli JA, Horwath RO, Gotou E, Satou K, Wu RJ, Bahl CP, Narang SA, Hershberger CL, Baxter JD, Roberts JL, Seeburg PH, Goodman HM, Tsuchida T. Patents and literature. Appl Biochem Biotechnol. 1982 Nov;7(6):497-510. doi: 10.1007/BF02799180. PMID: 24234462.
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Experimental and computational evidence for a boron-assisted, sigma-bond metathesis pathway for alkane borylation.

Journal of the American Chemical Society

Webster CE, Fan Y, Hall MB, Kunz D, Hartwig JF.
PMID: 12537470
J Am Chem Soc. 2003 Jan 29;125(4):858-9. doi: 10.1021/ja028394c.

Photoejection of one CO ligand from isolated CpM(CO)n+1BR2 (n = 1: M = Fe, Ru; n = 2: M = Mo,W; R2 = catecholate or pinacolate) compounds produces a coordinatively unsaturated 16 e- intermediate, a cyclic dioxaboryl transition metal...

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Webster CE, Fan Y, Hall MB, et al. Experimental and computational evidence for a boron-assisted, sigma-bond metathesis pathway for alkane borylation. J Am Chem Soc. 2003;125(4):858-9doi: 10.1021/ja028394c.
Webster, C. E., Fan, Y., Hall, M. B., Kunz, D., & Hartwig, J. F. (2003). Experimental and computational evidence for a boron-assisted, sigma-bond metathesis pathway for alkane borylation. Journal of the American Chemical Society, 125(4), 858-9. https://doi.org/10.1021/ja028394c
Webster, Charles Edwin, et al. "Experimental and computational evidence for a boron-assisted, sigma-bond metathesis pathway for alkane borylation." Journal of the American Chemical Society vol. 125,4 (2003): 858-9. doi: https://doi.org/10.1021/ja028394c
Webster CE, Fan Y, Hall MB, Kunz D, Hartwig JF. Experimental and computational evidence for a boron-assisted, sigma-bond metathesis pathway for alkane borylation. J Am Chem Soc. 2003 Jan 29;125(4):858-9. doi: 10.1021/ja028394c. PMID: 12537470.
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Direct observation of beta-aryl eliminations from Rh(I) alkoxides.

Journal of the American Chemical Society

Zhao P, Incarvito CD, Hartwig JF.
PMID: 16522075
J Am Chem Soc. 2006 Mar 15;128(10):3124-5. doi: 10.1021/ja058550q.

beta-Aryl eliminations from a series of rhodium(I) alkoxides to form rhodium aryl complexes and free ketones are reported. Tertiary phenylmethoxide complexes [Rh(PEt3)n(OCPhRR')] (n = 2, 3) were prepared via alcoholysis of {Rh(PEt3)2[N(SiMe3)2} by the corresponding alcohols HOCPhRR' in the...

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Zhao P, Incarvito CD, Hartwig JF. Direct observation of beta-aryl eliminations from Rh(I) alkoxides. J Am Chem Soc. 2006;128(10):3124-5doi: 10.1021/ja058550q.
Zhao, P., Incarvito, C. D., & Hartwig, J. F. (2006). Direct observation of beta-aryl eliminations from Rh(I) alkoxides. Journal of the American Chemical Society, 128(10), 3124-5. https://doi.org/10.1021/ja058550q
Zhao, Pinjing, et al. "Direct observation of beta-aryl eliminations from Rh(I) alkoxides." Journal of the American Chemical Society vol. 128,10 (2006): 3124-5. doi: https://doi.org/10.1021/ja058550q
Zhao P, Incarvito CD, Hartwig JF. Direct observation of beta-aryl eliminations from Rh(I) alkoxides. J Am Chem Soc. 2006 Mar 15;128(10):3124-5. doi: 10.1021/ja058550q. PMID: 16522075.
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Distinct electronic effects on reductive eliminations of symmetrical and unsymmetrical bis-aryl platinum complexes.

Journal of the American Chemical Society

Shekhar S, Hartwig JF.
PMID: 15469300
J Am Chem Soc. 2004 Oct 13;126(40):13016-27. doi: 10.1021/ja0480365.

Symmetrical bis-aryl platinum complexes (DPPF)Pt(C(6)H(4)-4-R)(2) (R = NMe(2), OMe, CH(3), H, Cl, CF(3)) and electronically unsymmetrical bis-aryl platinum complexes (DPPF)Pt(C(6)H(4)-4-R)(C(6)H(4)-4-X) (R = CH(3), X = NMe(2), OMe, H, Cl, F, CF(3); R = OMe, X = NMe(2), H, Cl,...

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Shekhar S, Hartwig JF. Distinct electronic effects on reductive eliminations of symmetrical and unsymmetrical bis-aryl platinum complexes. J Am Chem Soc. 2004;126(40):13016-27doi: 10.1021/ja0480365.
Shekhar, S., & Hartwig, J. F. (2004). Distinct electronic effects on reductive eliminations of symmetrical and unsymmetrical bis-aryl platinum complexes. Journal of the American Chemical Society, 126(40), 13016-27. https://doi.org/10.1021/ja0480365
Shekhar, Shashank, and Hartwig, John F. "Distinct electronic effects on reductive eliminations of symmetrical and unsymmetrical bis-aryl platinum complexes." Journal of the American Chemical Society vol. 126,40 (2004): 13016-27. doi: https://doi.org/10.1021/ja0480365
Shekhar S, Hartwig JF. Distinct electronic effects on reductive eliminations of symmetrical and unsymmetrical bis-aryl platinum complexes. J Am Chem Soc. 2004 Oct 13;126(40):13016-27. doi: 10.1021/ja0480365. PMID: 15469300.
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Interactions among Flavonoid nod Gene Inducers Released from Alfalfa Seeds and Roots.

Plant physiology

Hartwig UA, Maxwell CA, Joseph CM, Phillips DA.
PMID: 16667124
Plant Physiol. 1989 Nov;91(3):1138-42. doi: 10.1104/pp.91.3.1138.

Alfalfa (Medicago sativa L.) seeds and roots can create complex rhizosphere effects by releasing flavonoids that induce nodulation (nod) genes in Rhizobium meliloti. Previous reports identified luteolin and 4,4'-dihydroxy-2'-methoxychalcone as strong inducers that are released from seeds and roots,...

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Hartwig UA, Maxwell CA, Joseph CM, et al. Interactions among Flavonoid nod Gene Inducers Released from Alfalfa Seeds and Roots. Plant Physiol. 1989;91(3):1138-42doi: 10.1104/pp.91.3.1138.
Hartwig, U. A., Maxwell, C. A., Joseph, C. M., & Phillips, D. A. (1989). Interactions among Flavonoid nod Gene Inducers Released from Alfalfa Seeds and Roots. Plant physiology, 91(3), 1138-42. https://doi.org/10.1104/pp.91.3.1138
Hartwig, U A, et al. "Interactions among Flavonoid nod Gene Inducers Released from Alfalfa Seeds and Roots." Plant physiology vol. 91,3 (1989): 1138-42. doi: https://doi.org/10.1104/pp.91.3.1138
Hartwig UA, Maxwell CA, Joseph CM, Phillips DA. Interactions among Flavonoid nod Gene Inducers Released from Alfalfa Seeds and Roots. Plant Physiol. 1989 Nov;91(3):1138-42. doi: 10.1104/pp.91.3.1138. PMID: 16667124; PMCID: PMC1062131.
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