A chemoenzymatic total synthesis of (+)-amabiline

Alison D. Findlay; Martin G. Banwell

doi:10.1021/ol901230w

A chemoenzymatic total synthesis of (+)-amabiline

Alison D. Findlay, Martin G. Banwell

Research output: Contribution to journal › Article › peer-review

39 Citations (Scopus)

Abstract

The readily available and enzymatically derived cis-1,2-dihydrocatechol 3 has been converted, over 15 steps, into (+)-amabiline, the nonnatural enantiomeric form of a crinine-type alkaloid.

Original language	English
Pages (from-to)	3160-3162
Number of pages	3
Journal	Organic Letters
Volume	11
Issue number	14
DOIs	https://doi.org/10.1021/ol901230w
Publication status	Published - 16 Jul 2009

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title = "A chemoenzymatic total synthesis of (+)-amabiline",

abstract = "The readily available and enzymatically derived cis-1,2-dihydrocatechol 3 has been converted, over 15 steps, into (+)-amabiline, the nonnatural enantiomeric form of a crinine-type alkaloid.",

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JO - Organic Letters

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A chemoenzymatic total synthesis of (+)-amabiline

Abstract

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