✦ LIBER ✦

Highly stereoselective synthesis of antitumor agents: both enantiomers of goniothales diol, altholactone, and isoaltholactone

✍ Scribed by Jhillu Singh Yadav; Atcha Krishnam Raju; Ponugoti Purushothama Rao; Gurram Rajaiah

Book ID: 108283997
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 196 KB
Volume: 16
Category: Article
ISSN: 0957-4166
DOI: 10.1016/j.tetasy.2005.08.047

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A concise and stereoselective synthesis

A concise and stereoselective synthesis of both enantiomers of altholactone and isoaltholactone

✍ J.S. Yadav; G. Rajaiah; A.Krishnam Raju 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 236 KB

A concise and flexible stereoselective route to synthesize both enantiomers of the highly functionalized a,b-unsaturatedd-lactones, altholactone and isoaltholactone, from readily available cinnamyl alcohol is described. This approach derived its asymmetry from Sharpless catalytic asymmetric epoxidat

ChemInform Abstract: Highly Stereoselect

ChemInform Abstract: Highly Stereoselective Synthesis of Both Enantiomers of 2-Methyl-3- hydroxythioesters by Asymmetric Aldol Reactions Using Similar Types of Chiral Sources Derived from L-Proline.

✍ S. KOBAYASHI; M. HORIBE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB