Abstract
Synthesis of 2 diastereoisomers of A/B fragments of ciguatoxin was achieved by connecting a hexose and 2 pentose derivatives with silylacetylene. The key steps are the cationic cyclization and reductive decomplexation of the acetylene biscobalthexacarbonyl complex.
Original language | English |
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Pages (from-to) | 1179-1180 |
Number of pages | 2 |
Journal | Synlett |
Volume | 1995 |
Issue number | 11 |
DOIs | |
Publication status | Published - 1995 Nov 1 |
Externally published | Yes |
Keywords
- Two diastereoisomers were synthesized from D-glucose and D-arabinose or L-xylose derivatives as partial model compounds for the A/B ring of ciguatoxin.
ASJC Scopus subject areas
- Organic Chemistry