A new approach to the pseudopterosins using an arene alkylation with a γ-methylene-γ-butyrolactone
✍ Scribed by David C Harrowven; Jonathan D Wilden; Melloney J Tyte; Michael B Hursthouse; Simon J Coles
- Book ID
- 104211701
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 87 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A short and practical route to the tricyclic core of an unnatural pseudopterosin diastereoisomer is presented. Key features are an arene alkylation with a g-methylene-g-butyrolactone, viz. 1014, and an elaborate reduction sequence 1417 which both proceed diastereoselectively.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
The paper describes a new approach to the pseudopterosins i n which a sequential an%? alkylation with a tetrahydrofuran is used as a key step (viz. 2 + 1).