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Total synthesis of (2S,3R,5S)-(−)-2,3-dihydroxytetradecan-5-olide, a new biologically active δ-lactone produced by Seiridium unicorne

✍ Scribed by Hiroaki Toshima; Hiroji Sato; Akitami Ichihara

Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
632 KB
Volume
55
Category
Article
ISSN
0040-4020

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ChemInform Abstract: Total Synthesis of
ChemInform Abstract: Total Synthesis of (2S,3R,5S)-(-)-2,3-Dihydroxytetradecan-5-olide, a New Biologically Acitve δ-Lactone Produced by Seiridium unicorne.
✍ Hiroaki Toshima; Hiroji Sato; Akitami Ichihara 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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 first stereoselective total synthesi
The first stereoselective total synthesis of (3S,4R)-dihydroxy-(6S)-undecyl-α-pyranone and total synthesis of (2S,3R,5S)-(−)-2,3-dihydroxytetradecan-5-olide
✍ Gowravaram Sabitha; Sambit Nayak; M. Bhikshapathi; J.S. Yadav 📂 Article 📅 2009 🏛 Elsevier Science 🌐 French ⚖ 185 KB

The first total synthesis of (3S,4R)-dihydroxy-(6S)-undecyl-a-pyranone 1 and total synthesis of (2S,3R,5S)-(À)-2,3-dihydroxytetradecan-5-olide 2 have been achieved in five steps in a highly stereoselective manner using Maruoka allylation, olefin cross-metathesis, and Sharpless asymmetric dihydroxyla