Synthesis of the Prelog-Djerassi Lactone and Protomycinolide IV Based on the Stereospecific Methylation of γ,δ-Epoxy Acrylates by Trimethylaluminum
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/21/6/21_6_1101/_pdf
Reference14 articles.
1. Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis
2. Stereospecific methylation of .gamma.,.delta.-epoxy acrylates by trimethylaluminum: a method for the iterative construction of polypropionate chains
3. The Structure of the Antibiotic Methymycin1
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3. Trimethylaluminum;Encyclopedia of Reagents for Organic Synthesis;2017-09-06
4. Asymmetric Hydroformylation-Initiated Tandem Sequences for Syntheses of (+)-Patulolide C, (−)-Pyrenophorol, (+)-Decarestrictine L, and (+)-Prelog Djerassi Lactone;The Journal of Organic Chemistry;2014-12-01
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