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• W2106631634 endingPage "8853" @default.
• W2106631634 startingPage "8841" @default.
• W2106631634 abstract "[reaction: see text] Herein, we disclose our results regarding various strategies toward the assembly of the octanyl ring of vinigrol. Attempts to generate the problematic eight-membered ring through a ring expansion or via unification of the terminal olefins using the ring-closing metathesis were not successful. The cyclooctane ring was created via a sequential hydroxy Diels-Alder/Claisen rearrangement reaction of diene 55 and N-benzylmaleimide." @default.
• W2106631634 created "2016-06-24" @default.
• W2106631634 creator A5045304239 @default.
• W2106631634 creator A5085784374 @default.
• W2106631634 date "2005-09-24" @default.
• W2106631634 modified "2023-09-23" @default.
• W2106631634 title "Studies toward the Total Synthesis of Vinigrol. Synthesis of the Octalin Ring" @default.
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• W2106631634 doi "https://doi.org/10.1021/jo051318i" @default.
• W2106631634 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16238317" @default.
• W2106631634 hasPublicationYear "2005" @default.
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