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Cruciferous vegetables, isothiocyanates and indoles

evaluation

[No authors listed]
GSID: clegjEs4lYEJ
, … Working Group on the Evaluation of Cancer-Preventive … - 2004 - books.google.com

This publication sets outs the findings of an IARC Working Group, held in Lyon, France in November 2003, which considered the benefits of a diet rich in cruciferous vegetables in helping to reduce the risk of various cancers. Cruciferous...

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International Agency for Research on Cancer, IARC Working Group on the Evaluation of Cancer-Preventive Strategies, & World Health Organization. (2004). Cruciferous vegetables, isothiocyanates and indoles (No. 9). IARC.
International Agency for Research on Cancer, IARC Working Group on the Evaluation of Cancer-Preventive Strategies, and World Health Organization. Cruciferous vegetables, isothiocyanates and indoles. No. 9. IARC, 2004.
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Organizational change: An action-oriented toolkit

ADVANCE: Organizational Change for Gender Equity in STEM Academic Professions AND Program Evaluation

Ingols C.
GSID: NnkynHW-UaEJ
G Deszca, C Ingols, TF Cawsey - 2019 - books.google.com

" In today's world, organizational resilience, adaptability and agility gain new prominence. Awaken, mobilize, accelerate, and institutionalize change with Organizational Change: An Action-Oriented Toolkit, Fourth Edition. Bridging theory with practice, this new edition uses models, examples, and exercises to...

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Deszca, G., Ingols, C., & Cawsey, T. F. (2019). Organizational change: An action-oriented toolkit. Sage Publications.
Deszca, Gene, Cynthia Ingols, and Tupper F. Cawsey. Organizational change: An action-oriented toolkit. Sage Publications, 2019.
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IL-6 levels and genotype are associated with risk of young adult Hodgkin lymphoma

adult

Cozen W, Ingles SA.
GSID: _N8kkSi19yIJ
W Cozen, PS Gill, SA Ingles, R Masood… - Blood, 2004 - ashpublications.org

… Identical twins of young adult Hodgkin lymphoma case subjects are much more likely to … to young adult Hodgkin lymphoma. We obtained blood specimens from 88 young adult Hodgkin …

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Cozen, W., Gill, P. S., Ingles, S. A., Masood, R., Martínez-Maza, O., Cockburn, M. G., ... & Mack, T. M. (2004). IL-6 levels and genotype are associated with risk of young adult Hodgkin lymphoma. Blood, 103(8), 3216-3221.
Cozen, Wendy, et al. "IL-6 levels and genotype are associated with risk of young adult Hodgkin lymphoma." Blood 103.8 (2004): 3216-3221.
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"On water", phosphine-free palladium-catalyzed room temperature C-H arylation of indoles.

Chemistry (Weinheim an der Bergstrasse, Germany)

Islam S, Larrosa I.
PMID: 24123582
Chemistry. 2013 Nov 04;19(45):15093-6. doi: 10.1002/chem.201302838. Epub 2013 Oct 07.

No abstract available.

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Islam S, Larrosa I. "On water", phosphine-free palladium-catalyzed room temperature C-H arylation of indoles. Chemistry. 2013;19(45):15093-6doi: 10.1002/chem.201302838.
Islam, S., & Larrosa, I. (2013). "On water", phosphine-free palladium-catalyzed room temperature C-H arylation of indoles. Chemistry (Weinheim an der Bergstrasse, Germany), 19(45), 15093-6. https://doi.org/10.1002/chem.201302838
Islam, Saidul, and Larrosa, Igor. ""On water", phosphine-free palladium-catalyzed room temperature C-H arylation of indoles." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 19,45 (2013): 15093-6. doi: https://doi.org/10.1002/chem.201302838
Islam S, Larrosa I. "On water", phosphine-free palladium-catalyzed room temperature C-H arylation of indoles. Chemistry. 2013 Nov 04;19(45):15093-6. doi: 10.1002/chem.201302838. Epub 2013 Oct 07. PMID: 24123582.
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Pd-Catalyzed Intramolecular Cyclization via Direct C-H Addition to Nitriles: Skeletal Diverse Synthesis of Fused Polycyclic Indoles.

Organic letters

Wang TT, Zhao L, Zhang YJ, Liao WW.
PMID: 27626643
Org Lett. 2016 Oct 07;18(19):5002-5005. doi: 10.1021/acs.orglett.6b02460. Epub 2016 Sep 14.

The first example of Pd-catalyzed intramolecular C-H addition of indoles bearing cyanohydrin components at the C(3), C(2), and N(1) positions to nitriles is described. A wide range of functionalized partially saturated carbazoles, tetrahydropyrido[1,2-a]indole, and carbazoles can be prepared in...

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Wang TT, Zhao L, Zhang YJ, et al. Pd-Catalyzed Intramolecular Cyclization via Direct C-H Addition to Nitriles: Skeletal Diverse Synthesis of Fused Polycyclic Indoles. Org Lett. 2016;18(19):5002-5005doi: 10.1021/acs.orglett.6b02460.
Wang, T. T., Zhao, L., Zhang, Y. J., & Liao, W. W. (2016). Pd-Catalyzed Intramolecular Cyclization via Direct C-H Addition to Nitriles: Skeletal Diverse Synthesis of Fused Polycyclic Indoles. Organic letters, 18(19), 5002-5005. https://doi.org/10.1021/acs.orglett.6b02460
Wang, Ting-Ting, et al. "Pd-Catalyzed Intramolecular Cyclization via Direct C-H Addition to Nitriles: Skeletal Diverse Synthesis of Fused Polycyclic Indoles." Organic letters vol. 18,19 (2016): 5002-5005. doi: https://doi.org/10.1021/acs.orglett.6b02460
Wang TT, Zhao L, Zhang YJ, Liao WW. Pd-Catalyzed Intramolecular Cyclization via Direct C-H Addition to Nitriles: Skeletal Diverse Synthesis of Fused Polycyclic Indoles. Org Lett. 2016 Oct 07;18(19):5002-5005. doi: 10.1021/acs.orglett.6b02460. Epub 2016 Sep 14. PMID: 27626643.
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Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles.

Organic letters

Jung Y, Kim I.
PMID: 26345614
Org Lett. 2015 Sep 18;17(18):4600-3. doi: 10.1021/acs.orglett.5b02331. Epub 2015 Sep 08.

Attempted cyclization of indolizines bearing both formyl and alkyne groups under acid catalysis provided benzo[e]pyrido[1,2-a]indoles with an aryl substituent at the C6 position as major products, along with the expected C5-acylated benzo[e]pyrido[1,2-a]indoles as minor ones, which resulted from preferential...

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Jung Y, Kim I. Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles. Org Lett. 2015;17(18):4600-3doi: 10.1021/acs.orglett.5b02331.
Jung, Y., & Kim, I. (2015). Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles. Organic letters, 17(18), 4600-3. https://doi.org/10.1021/acs.orglett.5b02331
Jung, Youngeun, and Kim, Ikyon. "Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles." Organic letters vol. 17,18 (2015): 4600-3. doi: https://doi.org/10.1021/acs.orglett.5b02331
Jung Y, Kim I. Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles. Org Lett. 2015 Sep 18;17(18):4600-3. doi: 10.1021/acs.orglett.5b02331. Epub 2015 Sep 08. PMID: 26345614.
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σ-π Continuum in Indole-Palladium(II) Complexes.

Angewandte Chemie (International ed. in English)

Yamamoto K, Kimura S, Murahashi T.
PMID: 27008579
Angew Chem Int Ed Engl. 2016 Apr 18;55(17):5322-6. doi: 10.1002/anie.201601992. Epub 2016 Mar 23.

The intrinsic features of (hetero-arene)-metal interactions have been elusive mainly because the systematic structure analysis of non-anchored hetero-arene-metal complexes has been hampered by their labile nature. We report successful isolation and systematic structure analysis of a series of non-anchored...

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Yamamoto K, Kimura S, Murahashi T. σ-π Continuum in Indole-Palladium(II) Complexes. Angew Chem Int Ed Engl. 2016;55(17):5322-6doi: 10.1002/anie.201601992.
Yamamoto, K., Kimura, S., & Murahashi, T. (2016). σ-π Continuum in Indole-Palladium(II) Complexes. Angewandte Chemie (International ed. in English), 55(17), 5322-6. https://doi.org/10.1002/anie.201601992
Yamamoto, Koji, et al. "σ-π Continuum in Indole-Palladium(II) Complexes." Angewandte Chemie (International ed. in English) vol. 55,17 (2016): 5322-6. doi: https://doi.org/10.1002/anie.201601992
Yamamoto K, Kimura S, Murahashi T. σ-π Continuum in Indole-Palladium(II) Complexes. Angew Chem Int Ed Engl. 2016 Apr 18;55(17):5322-6. doi: 10.1002/anie.201601992. Epub 2016 Mar 23. PMID: 27008579.
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Ruthenium(II)-Catalyzed Redox-Neutral [3+2] Annulation of Indoles with Internal Alkynes via C-H Bond Activation: Accessing a Pyrroloindolone Scaffold.

The Journal of organic chemistry

Xie Y, Wu X, Li C, Wang J, Li J, Liu H.
PMID: 28421753
J Org Chem. 2017 May 19;82(10):5263-5273. doi: 10.1021/acs.joc.7b00575. Epub 2017 May 02.

Ru(II)-catalyzed redox-neutral [3+2] annulation reactions of N-ethoxycarbamoyl indoles and internal alkynes via C-H bond activation are reported. This method features a broad internal alkyne scope, including various aryl/alkyl-, alkyl/alkyl-, and diaryl-substituted alkynes, good to excellent regioselectivity, diverse functional group...

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Xie Y, Wu X, Li C, et al. Ruthenium(II)-Catalyzed Redox-Neutral [3+2] Annulation of Indoles with Internal Alkynes via C-H Bond Activation: Accessing a Pyrroloindolone Scaffold. J Org Chem. 2017;82(10):5263-5273doi: 10.1021/acs.joc.7b00575.
Xie, Y., Wu, X., Li, C., Wang, J., Li, J., & Liu, H. (2017). Ruthenium(II)-Catalyzed Redox-Neutral [3+2] Annulation of Indoles with Internal Alkynes via C-H Bond Activation: Accessing a Pyrroloindolone Scaffold. The Journal of organic chemistry, 82(10), 5263-5273. https://doi.org/10.1021/acs.joc.7b00575
Xie, Yanan, et al. "Ruthenium(II)-Catalyzed Redox-Neutral [3+2] Annulation of Indoles with Internal Alkynes via C-H Bond Activation: Accessing a Pyrroloindolone Scaffold." The Journal of organic chemistry vol. 82,10 (2017): 5263-5273. doi: https://doi.org/10.1021/acs.joc.7b00575
Xie Y, Wu X, Li C, Wang J, Li J, Liu H. Ruthenium(II)-Catalyzed Redox-Neutral [3+2] Annulation of Indoles with Internal Alkynes via C-H Bond Activation: Accessing a Pyrroloindolone Scaffold. J Org Chem. 2017 May 19;82(10):5263-5273. doi: 10.1021/acs.joc.7b00575. Epub 2017 May 02. PMID: 28421753.
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Manganese(I)-Catalyzed Direct C-H Allylation of Arenes with Allenes.

The Journal of organic chemistry

Chen SY, Li Q, Wang H.
PMID: 28948781
J Org Chem. 2017 Oct 20;82(20):11173-11181. doi: 10.1021/acs.joc.7b02220. Epub 2017 Oct 03.

Polysubstituted allyl groups, for example, the prenyl group, are valuable synthetic handles and widely encountered in bioactive compounds. Reported herein is a manganese(I)-catalyzed direct C-H coupling with allenes for the efficient assembly of allylated arenes. The protocol offers an...

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Chen SY, Li Q, Wang H. Manganese(I)-Catalyzed Direct C-H Allylation of Arenes with Allenes. J Org Chem. 2017;82(20):11173-11181doi: 10.1021/acs.joc.7b02220.
Chen, S. Y., Li, Q., & Wang, H. (2017). Manganese(I)-Catalyzed Direct C-H Allylation of Arenes with Allenes. The Journal of organic chemistry, 82(20), 11173-11181. https://doi.org/10.1021/acs.joc.7b02220
Chen, Shi-Yong, et al. "Manganese(I)-Catalyzed Direct C-H Allylation of Arenes with Allenes." The Journal of organic chemistry vol. 82,20 (2017): 11173-11181. doi: https://doi.org/10.1021/acs.joc.7b02220
Chen SY, Li Q, Wang H. Manganese(I)-Catalyzed Direct C-H Allylation of Arenes with Allenes. J Org Chem. 2017 Oct 20;82(20):11173-11181. doi: 10.1021/acs.joc.7b02220. Epub 2017 Oct 03. PMID: 28948781.
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Prevalence of Functional Problems After Oral Cavity Malignancy Treatment at a Tertiary Center: Utilizing PSS HN (Performance Status Scale for Head and Neck) Scale.

Journal of maxillofacial and oral surgery

Yadav K, Nair D, Agarwal J, Chakrabarti S, Joshi S, Ingole P, Mishra A, Tathe N, Chaturvedi P.
PMID: 26929551
J Maxillofac Oral Surg. 2016 Mar;15(1):38-44. doi: 10.1007/s12663-015-0805-2. Epub 2015 Jun 04.

BACKGROUND: Oral cancer is the most common type of cancer occurring in India and it is equally important to assess morbidities after treatment for optimal utilization of resources. Utilizing PSS HN we try to identify the patient population who...

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Yadav K, Nair D, Agarwal J, et al. Prevalence of Functional Problems After Oral Cavity Malignancy Treatment at a Tertiary Center: Utilizing PSS HN (Performance Status Scale for Head and Neck) Scale. J Maxillofac Oral Surg. 2015;15(1):38-44doi: 10.1007/s12663-015-0805-2.
Yadav, K., Nair, D., Agarwal, J., Chakrabarti, S., Joshi, S., Ingole, P., Mishra, A., Tathe, N., & Chaturvedi, P. (2016). Prevalence of Functional Problems After Oral Cavity Malignancy Treatment at a Tertiary Center: Utilizing PSS HN (Performance Status Scale for Head and Neck) Scale. Journal of maxillofacial and oral surgery, 15(1), 38-44. https://doi.org/10.1007/s12663-015-0805-2
Yadav, Kaushal, et al. "Prevalence of Functional Problems After Oral Cavity Malignancy Treatment at a Tertiary Center: Utilizing PSS HN (Performance Status Scale for Head and Neck) Scale." Journal of maxillofacial and oral surgery vol. 15,1 (2016): 38-44. doi: https://doi.org/10.1007/s12663-015-0805-2
Yadav K, Nair D, Agarwal J, Chakrabarti S, Joshi S, Ingole P, Mishra A, Tathe N, Chaturvedi P. Prevalence of Functional Problems After Oral Cavity Malignancy Treatment at a Tertiary Center: Utilizing PSS HN (Performance Status Scale for Head and Neck) Scale. J Maxillofac Oral Surg. 2016 Mar;15(1):38-44. doi: 10.1007/s12663-015-0805-2. Epub 2015 Jun 04. PMID: 26929551; PMCID: PMC4759033.
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Iridium-Catalyzed Asymmetric Allylic Dearomatization by a Desymmetrization Strategy.

Angewandte Chemie (International ed. in English)

Wang Y, Zheng C, You SL.
PMID: 28980373
Angew Chem Int Ed Engl. 2017 Nov 20;56(47):15093-15097. doi: 10.1002/anie.201708419. Epub 2017 Oct 24.

A desymmetrization strategy was developed involving iridium-catalyzed allylic dearomatization of indoles. The six-membered-ring spiroindolenines contain three contiguous stereogenic centers, including an all-carbon quaternary center, and were obtained in up to 99 % yield with 99 % ee and >95:5...

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Wang Y, Zheng C, You SL. Iridium-Catalyzed Asymmetric Allylic Dearomatization by a Desymmetrization Strategy. Angew Chem Int Ed Engl. 2017;56(47):15093-15097doi: 10.1002/anie.201708419.
Wang, Y., Zheng, C., & You, S. L. (2017). Iridium-Catalyzed Asymmetric Allylic Dearomatization by a Desymmetrization Strategy. Angewandte Chemie (International ed. in English), 56(47), 15093-15097. https://doi.org/10.1002/anie.201708419
Wang, Ye, et al. "Iridium-Catalyzed Asymmetric Allylic Dearomatization by a Desymmetrization Strategy." Angewandte Chemie (International ed. in English) vol. 56,47 (2017): 15093-15097. doi: https://doi.org/10.1002/anie.201708419
Wang Y, Zheng C, You SL. Iridium-Catalyzed Asymmetric Allylic Dearomatization by a Desymmetrization Strategy. Angew Chem Int Ed Engl. 2017 Nov 20;56(47):15093-15097. doi: 10.1002/anie.201708419. Epub 2017 Oct 24. PMID: 28980373.
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Iron-Mediated Domino Interrupted Iso-Nazarov/Dearomative (3 + 2)-Cycloaddition of Electrophilic Indoles.

Organic letters

Marques AS, Coeffard V, Chataigner I, Vincent G, Moreau X.
PMID: 27700117
Org Lett. 2016 Oct 21;18(20):5296-5299. doi: 10.1021/acs.orglett.6b02613. Epub 2016 Oct 04.

An efficient domino reaction combining different classes of pericyclic reactions leads to chiral complex polycyclic indoline-based architectures from achiral starting materials under mild conditions. This practical method is based on the ability of iron(III) chloride to promote both 4π...

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Marques AS, Coeffard V, Chataigner I, et al. Iron-Mediated Domino Interrupted Iso-Nazarov/Dearomative (3 + 2)-Cycloaddition of Electrophilic Indoles. Org Lett. 2016;18(20):5296-5299doi: 10.1021/acs.orglett.6b02613.
Marques, A. S., Coeffard, V., Chataigner, I., Vincent, G., & Moreau, X. (2016). Iron-Mediated Domino Interrupted Iso-Nazarov/Dearomative (3 + 2)-Cycloaddition of Electrophilic Indoles. Organic letters, 18(20), 5296-5299. https://doi.org/10.1021/acs.orglett.6b02613
Marques, Anne-Sophie, et al. "Iron-Mediated Domino Interrupted Iso-Nazarov/Dearomative (3 + 2)-Cycloaddition of Electrophilic Indoles." Organic letters vol. 18,20 (2016): 5296-5299. doi: https://doi.org/10.1021/acs.orglett.6b02613
Marques AS, Coeffard V, Chataigner I, Vincent G, Moreau X. Iron-Mediated Domino Interrupted Iso-Nazarov/Dearomative (3 + 2)-Cycloaddition of Electrophilic Indoles. Org Lett. 2016 Oct 21;18(20):5296-5299. doi: 10.1021/acs.orglett.6b02613. Epub 2016 Oct 04. PMID: 27700117.
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Showing 1 to 12 of 2303 entries