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Enantioselective Synthesis of the Ester Side Chain of Homoharringtonine

✍ Scribed by Laurent Keller; Françoise Dumas; Jean d’Angelo

Book ID
102176740
Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
202 KB
Volume
2003
Category
Article
ISSN
1434-193X

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📜 SIMILAR VOLUMES

Enantioselective synthesis of the ester
Enantioselective synthesis of the ester side chain of homoharringtonine
✍ Laurent Keller; Françoise Dumas; Jean d'Angelo 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 89 KB

The Michael adduct 6 was converted in ten steps with an overall yield of 5.7% into the methyl ester derivative of the side chain of homoharringtonine, (R)-17.

ChemInform Abstract: Enantioselective Sy
ChemInform Abstract: Enantioselective Synthesis of the Ester Side Chain of Homoharringtonine (IX).
✍ Laurent Keller; Francoise Dumas; Jean d'Angelo 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 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

Construction of Chiral Tertiary Alcohol
Construction of Chiral Tertiary Alcohol Stereocenters via the [2,3]- Meisenheimer Rearrangement: Enantioselective Synthesis of the Side-Chain Acids of Homoharringtonine and Harringtonine
✍ Yang, Hua; Sun, Moran; Zhao, Shuguang; Zhu, Ming; Xie, Yangla; Niu, Changling; L 📂 Article 📅 2012 🏛 American Chemical Society 🌐 English ⚖ 645 KB

For the first time, the [2,3]-Meisenheimer rearrangement has been developed into a general strategy for the construction of chiral tertiary alcohols. The effectiveness and practicality of this methodology are illustrated by the successful synthesis of (R)-20 and (R)-30, the side chain acids of homoh