Namjoshi OA - Search Results

1

Base-mediated stereospecific synthesis of aryloxy and amino substituted ethyl acrylates.

Kabir MS, Namjoshi OA, Verma R, Lorenz M, Tiruveedhula VV, Monte A, Bertz SH, Schwabacher AW, Cook JM. Kabir MS, et al. Among authors: namjoshi oa. J Org Chem. 2012 Jan 6;77(1):300-10. doi: 10.1021/jo201948e. Epub 2011 Nov 28. J Org Chem. 2012. PMID: 22073965 Free PMC article.

2

First application of an efficient and versatile ligand for copper-catalyzed cross-coupling reactions of vinyl halides with N-heterocycles and phenols.

Kabir MS, Lorenz M, Namjoshi OA, Cook JM. Kabir MS, et al. Among authors: namjoshi oa. Org Lett. 2010 Feb 5;12(3):464-7. doi: 10.1021/ol9026446. Org Lett. 2010. PMID: 20039699 Free PMC article.

3

A very active cu-catalytic system for the synthesis of aryl, heteroaryl, and vinyl sulfides.

Kabir MS, Lorenz M, Van Linn ML, Namjoshi OA, Ara S, Cook JM. Kabir MS, et al. Among authors: namjoshi oa. J Org Chem. 2010 Jun 4;75(11):3626-43. doi: 10.1021/jo1004179. J Org Chem. 2010. PMID: 20429581

4

A new class of potential anti-tuberculosis agents: Synthesis and preliminary evaluation of novel acrylic acid ethyl ester derivatives.

Kabir MS, Namjoshi OA, Verma R, Polanowski R, Krueger SM, Sherman D, Rott MA, Schwan WR, Monte A, Cook JM. Kabir MS, et al. Among authors: namjoshi oa. Bioorg Med Chem. 2010 Jun 15;18(12):4178-86. doi: 10.1016/j.bmc.2010.05.016. Epub 2010 May 7. Bioorg Med Chem. 2010. PMID: 20537903

5

Stereospecific approach to the synthesis of ring-A oxygenated sarpagine indole alkaloids. Total synthesis of the dimeric indole alkaloid P-(+)-dispegatrine and six other monomeric indole alkaloids.

Edwankar CR, Edwankar RV, Namjoshi OA, Liao X, Cook JM. Edwankar CR, et al. Among authors: namjoshi oa. J Org Chem. 2013 Jul 5;78(13):6471-87. doi: 10.1021/jo400469t. Epub 2013 Jun 18. J Org Chem. 2013. PMID: 23721107 Free PMC article.

6

Stereospecific total synthesis of the indole alkaloid ervincidine. Establishment of the C-6 hydroxyl stereochemistry.

Rallapalli SK, Namjoshi OA, Tiruveedhula VV, Deschamps JR, Cook JM. Rallapalli SK, et al. Among authors: namjoshi oa. J Org Chem. 2014 May 2;79(9):3776-80. doi: 10.1021/jo402692u. Epub 2014 Apr 18. J Org Chem. 2014. PMID: 24697213 Free PMC article.

7

Development of a two-step route to 3-PBC and βCCt, two agents active against alcohol self-administration in rodent and primate models.

Namjoshi OA, Gryboski A, Fonseca GO, Van Linn ML, Wang ZJ, Deschamps JR, Cook JM. Namjoshi OA, et al. J Org Chem. 2011 Jun 3;76(11):4721-7. doi: 10.1021/jo200425m. Epub 2011 May 4. J Org Chem. 2011. PMID: 21495660 Free PMC article.

8

Sarpagine and Related Alkaloids.

Namjoshi OA, Cook JM. Namjoshi OA, et al. Alkaloids Chem Biol. 2016;76:63-169. doi: 10.1016/bs.alkal.2015.08.002. Epub 2015 Oct 9. Alkaloids Chem Biol. 2016. PMID: 26827883 Free PMC article. Review.

9

Recent progress in the total synthesis of indole alkaloids.

Edwankar CR, Edwankar RV, Namjoshi OA, Rallapalli SK, Yang J, Cook JM. Edwankar CR, et al. Among authors: namjoshi oa. Curr Opin Drug Discov Devel. 2009 Nov;12(6):752-71. Curr Opin Drug Discov Devel. 2009. PMID: 19894188 Review.

10

Design, synthesis, and subtype selectivity of 3,6-disubstituted β-carbolines at Bz/GABA(A)ergic receptors. SAR and studies directed toward agents for treatment of alcohol abuse.

Yin W, Majumder S, Clayton T, Petrou S, VanLinn ML, Namjoshi OA, Ma C, Cromer BA, Roth BL, Platt DM, Cook JM. Yin W, et al. Among authors: namjoshi oa. Bioorg Med Chem. 2010 Nov 1;18(21):7548-64. doi: 10.1016/j.bmc.2010.08.049. Epub 2010 Sep 29. Bioorg Med Chem. 2010. PMID: 20888240 Free PMC article.

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