Cook JM - Search Results

1

First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A.

Yin W, Ma J, Rivas FM, Cook JM. Yin W, et al. Among authors: cook jm. Org Lett. 2007 Jan 18;9(2):295-8. doi: 10.1021/ol062762q. Org Lett. 2007. PMID: 17217288

2

Enantiospecific total synthesis of the sarpagine related indole alkaloids talpinine and talcarpine as well as the improved total synthesis of alstonerine and anhydromacrosalhine-methine via the asymmetric Pictet-Spengler reaction.

Yu P, Wang T, Li J, Cook JM. Yu P, et al. Among authors: cook jm. J Org Chem. 2000 May 19;65(10):3173-91. doi: 10.1021/jo000126e. J Org Chem. 2000. PMID: 10814213

3

General approach for the synthesis of sarpagine/ajmaline indole alkaloids. Stereospecific total synthesis of the sarpagine alkaloid (+)-vellosimine.

Wang T, Cook JM. Wang T, et al. Among authors: cook jm. Org Lett. 2000 Jul 13;2(14):2057-9. doi: 10.1021/ol000095+. Org Lett. 2000. PMID: 10891229

4

Stereocontrolled conversion of quinine into 10(R),11-dihydroxydihydroquinine via the sharpless osmylation process.

Zheng T, Flippen-Anderson J, Yu P, Wang T, Mirghani R, Cook JM. Zheng T, et al. Among authors: cook jm. J Org Chem. 2001 Feb 23;66(4):1509-11. doi: 10.1021/jo0015321. J Org Chem. 2001. PMID: 11312991 No abstract available.

5

Efficient asymmetric synthesis of biologically important tryptophan analogues via a palladium-mediated heteroannulation reaction.

Ma C, Liu X, Li X, Flippen-Anderson J, Yu S, Cook JM. Ma C, et al. Among authors: cook jm. J Org Chem. 2001 Jun 29;66(13):4525-42. doi: 10.1021/jo001679s. J Org Chem. 2001. PMID: 11421771

6

Stereocontrolled total synthesis of alkaloid G via the oxy-anion Cope rearrangement and improved total synthesis of (+)-ajmaline.

Wang T, Xu Q, Yu P, Liu X, Cook JM. Wang T, et al. Among authors: cook jm. Org Lett. 2001 Feb 8;3(3):345-8. doi: 10.1021/ol000331g. Org Lett. 2001. PMID: 11428010

7

General approach for the synthesis of sarpagine/macroline indole alkaloids. Enantiospecific total synthesis of the indole alkaloid trinervine.

Liu X, Cook JM. Liu X, et al. Among authors: cook jm. Org Lett. 2001 Dec 13;3(25):4023-6. doi: 10.1021/ol0101990. Org Lett. 2001. PMID: 11735575

8

Enantiospecific, stereospecific total synthesis of (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-N(a)-methylsarpagine as well as the total synthesis of the Alstonia bisindole macralstonidine.

Zhao S, Liao X, Cook JM. Zhao S, et al. Among authors: cook jm. Org Lett. 2002 Mar 7;4(5):687-90. doi: 10.1021/ol010222h. Org Lett. 2002. PMID: 11869102

9

Regiospecific, enantiospecific total synthesis of the alkoxy-substituted indole bases, 16-epi-N(a)-methylgardneral, 11-methoxyaffinisine, and 11-methoxymacroline as well as the indole alkaloids alstophylline and macralstonine.

Liu X, Deschamp JR, Cook JM. Liu X, et al. Among authors: cook jm. Org Lett. 2002 Oct 3;4(20):3339-42. doi: 10.1021/ol020101x. Org Lett. 2002. PMID: 12323013

10

Enantiospecific, stereospecific total synthesis of the oxindole alkaloid alstonisine.

Wearing XZ, Cook JM. Wearing XZ, et al. Among authors: cook jm. Org Lett. 2002 Nov 28;4(24):4237-40. doi: 10.1021/ol020170b. Org Lett. 2002. PMID: 12443067

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