Total Synthesis of (−)-Enigmazole A
A highly convergent, stereocontrolled total synthesis of the architecturally complex marine sponge metabolite (−)-enigmazole A has been achieved. Highlights include an unprecedented late-stage large-fragment Petasis–Ferrier union/rearrangement, a multicomponent Type I Anion Relay Chemistry (ARC) tac...
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Veröffentlicht in: | Journal of the American Chemical Society 2015-12, Vol.137 (49), p.15426-15429 |
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container_title | Journal of the American Chemical Society |
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creator | Ai, Yanran Kozytska, Mariya V Zou, Yike Khartulyari, Anton S Smith, Amos B |
description | A highly convergent, stereocontrolled total synthesis of the architecturally complex marine sponge metabolite (−)-enigmazole A has been achieved. Highlights include an unprecedented late-stage large-fragment Petasis–Ferrier union/rearrangement, a multicomponent Type I Anion Relay Chemistry (ARC) tactic, and a dithiane–epoxide union in conjunction with an oxazole-directed stereoselective reduction. |
doi_str_mv | 10.1021/jacs.5b11540 |
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source | ACS Publications; MEDLINE |
subjects | Communication Macrolides - chemical synthesis Macrolides - chemistry metabolites Molecular Structure Organophosphorus Compounds - chemical synthesis Organophosphorus Compounds - chemistry Oxazoles - chemical synthesis Oxazoles - chemistry Porifera stereochemistry |
title | Total Synthesis of (−)-Enigmazole A |
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