Article: Origin of the Thiopyrone CTP-431 “Unexpectedly” Isolated from the Marine Sponge Cacospongia mycofijiensis
Journal of organic chemistry. 2018 July 25, v. 83, no. 17
2018
Abstract: An intriguing hypothesis that latrunculin A, a well-known natural product, might have undergone transformation into the unprecedented thiopyrone CTP-431 upon long-term storage in methanol is advanced. Thus, opening of the hemiacetal of latrunculin A, ... ...
Abstract | An intriguing hypothesis that latrunculin A, a well-known natural product, might have undergone transformation into the unprecedented thiopyrone CTP-431 upon long-term storage in methanol is advanced. Thus, opening of the hemiacetal of latrunculin A, followed by E1CB elimination, and dehydration would give a polyene that could undergo intramolecular Diels–Alder reaction, followed by methanolysis of the thiazolidinone ring and ring closure by intramolecular thiol addition to an enone. Experimental evidence that the novel thiazolidinone to thiopyrone rearrangement can occur is presented. |
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Keywords | chemical structure ; methanol ; methanolysis ; organic chemistry ; Porifera ; storage ; thiols |
Language | English |
Dates of publication | 2018-0725 |
Size | p. 10595-10601. |
Publishing place | American Chemical Society |
Document type | Article |
ZDB-ID | 123490-0 |
ISSN | 1520-6904 ; 0022-3263 |
ISSN (online) | 1520-6904 |
ISSN | 0022-3263 |
DOI | 10.1021/acs.joc.8b01258 |
Database | NAL-Catalogue (AGRICOLA) |
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