| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219069 | Tetrahedron | 2012 | 4 Pages |
Abstract
The total synthesis of sapinofuranone A has been achieved starting from naturally occurring carbohydrate d-ribose via a short and high yielding route. The key transformations include Wittig olefination, Ohira-Bestmann reaction, Sonogashira coupling. Finally acetonide deprotection and subsequent lactonization using catalytic amount of hydrochloric acid completed the total synthesis of sapinofuranone A.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lingaiah Nagarapu, Shuklachary Karnakanti, Rajashaker Bantu,