Sub-structure syntheses and relative stereochemistry in the bistramide (bistratene) series of marine metabolites
| Data(s) |
01/01/2002
|
|---|---|
| Resumo |
The (6R*,9S*,11S*) and (22S*,23R*,27R*,31R*) stereochemistry, respectively, of the tetrahydropyranyl and spiroacetal moieties in bistramide A (1) have been established by stereoselective syntheses and high field NMR comparisons. Routes to the gamma-amino acid moiety are outlined. (C) 2002 Elsevier Science Ltd. All rights reserved. |
| Identificador | |
| Idioma(s) |
eng |
| Publicador |
Pergamon-Elsevier |
| Palavras-Chave | #Chemistry, Organic #Lissoclinum-bistratum #Spiroacetals #Carbon #Differentiation #Herboxidiene #Sluiter #C1 #250301 Organic Chemical Synthesis #250302 Biological and Medical Chemistry #780103 Chemical sciences #0305 Organic Chemistry |
| Tipo |
Journal Article |
