Cook JM - Search Results

1

Concise Total Synthesis of (-)-Affinisine Oxindole, (+)-Isoalstonisine, (+)-Alstofoline, (-)-Macrogentine, (+)-N_a -Demethylalstonisine, (-)-Alstonoxine A, and (+)-Alstonisine.

Stephen MR, Rahman MT, Tiruveedhula VVNPB, Fonseca GO, Deschamps JR, Cook JM. Stephen MR, et al. Among authors: cook jm. Chemistry. 2017 Nov 7;23(62):15805-15819. doi: 10.1002/chem.201703572. Epub 2017 Oct 18. Chemistry. 2017. PMID: 28875520 Free PMC article.

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

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

5

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

6

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

7

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

8

Stereospecific, enantiospecific total synthesis of the sarpagine indole alkaloids (E)16-epiaffinisine, (E)16-epinormacusine B, and dehydro-16-epiaffinisine.

Yu J, Liao X, Cook JM. Yu J, et al. Among authors: cook jm. Org Lett. 2002 Dec 26;4(26):4681-4. doi: 10.1021/ol020209c. Org Lett. 2002. PMID: 12489960

9

Enantiospecific total synthesis of (-)-(E)16-epiaffinisine, (+)-(E)16-epinormacusine B, and (+)-dehydro-16-epiaffinisine as well as the stereocontrolled total synthesis of alkaloid G.

Yu J, Wang T, Wearing XZ, Ma J, Cook JM. Yu J, et al. Among authors: cook jm. J Org Chem. 2003 Jul 25;68(15):5852-9. doi: 10.1021/jo030116o. J Org Chem. 2003. PMID: 12868917

10

The enantiospecific, stereospecific total synthesis of the ring-A oxygenated sarpagine indole alkaloids (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-N(a)-methylsarpagine, as well as the total synthesis of the alstonia bisindole alkaloid macralstonidine.

Zhao S, Liao X, Wang T, Flippen-Anderson J, Cook JM. Zhao S, et al. Among authors: cook jm. J Org Chem. 2003 Aug 8;68(16):6279-95. doi: 10.1021/jo030055u. J Org Chem. 2003. PMID: 12895062

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