Výsledky vyhledávání - "ARBORESCIDINE C"

Enantioselective total synthesis of (+)-arborescidine C and related tetracyclic indole alkaloids using organocatalysis

Autor: Vishal M. Sheth, Bor-Cherng Hong, Gene-Hsiang Lee

Publikováno v: Organic & Biomolecular Chemistry. 15:3408-3412

A concise and enantioselective synthesis of the tetracyclic indoles, including the naturally occurring compounds (+)-arborescidine C and (+)-arborescidine B, was achieved by the key step of Pictet-Spengler cyclization reaction with a Jacobsen-type th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cddb2ed85a20e8c5fca1248220f3b31
https://doi.org/10.1039/c7ob00473g

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Enantioselective Total Syntheses of (+)-Arborescidine A, (−)-Arborescidine B, and (−)-Arborescidine C

Autor: Viresh H. Rawal, Leonardo S. Santos, Ronaldo A. Pilli

Publikováno v: The Journal of Organic Chemistry. 69:1283-1289

Described are the first enantioselective total syntheses of (+)-arborescidine A ((+)-1), (-)-arborescidine B ((-)-2), and (-)-arborescidine C ((-)-3), via routes that proceeded in five steps and 50% overall yield, eight steps and 61% overall yield, a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24e2407e91704eab65ca9286ae479d29
https://doi.org/10.1021/jo035165f

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Akademický článek

Enantioselective Total Syntheses of (+)-Arborescidine A, (-)-Arborescidine B, and (-)-Arborescidine C.

Autor: Santos, Leonardo S., Pilli, Ronaldo A., Rawal, Viresh H.

Publikováno v: Journal of Organic Chemistry; 2/20/2004, Vol. 69 Issue 4, p1283-1289, 7p, 7 Diagrams

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Enantioselective Total Syntheses of (+)-Arborescidine A, (-)-Arborescidine B, and (-)-Arborescidine C

Autor: Viresh H. Rawal, Ronaldo A. Pilli, Leonardo S. Santos

Publikováno v: ChemInform. 35

Described are the first enantioselective total syntheses of (+)-arborescidine A ((+)-1), (−)-arborescidine B ((−)-2), and (−)-arborescidine C ((−)-3), via routes that proceeded in five steps and 50% overall yield, eight steps and 61% overall

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6faa91cd15a8fb2ac0f121e27763f2a6
https://doi.org/10.1002/chin.200429188

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