𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Asymmetric Synthesis of Quaternary Centers. Total Synthesis of (−)-Malyngolide

✍ Scribed by Trost, Barry M.; Tang, Weiping; Schulte, Jörg L.

Book ID
126775722
Publisher
American Chemical Society
Year
2000
Tongue
English
Weight
49 KB
Volume
2
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Asymmetric hetero Diels–Alder route to q
Asymmetric hetero Diels–Alder route to quaternary carbon centers: synthesis of (−)-malyngolide
✍ Arun K Ghosh; Michio Shirai 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 103 KB

Conformationally constrained chiral bis(oxazoline)-metal complex catalyzed asymmetric hetero Diels-Alder reactions of Danishefsky's diene and a variety of α-keto esters constructed quaternary carbon centers enantioselectively. The reaction was utilized in the synthesis of (-)-malyngolide.

ChemInform Abstract: Asymmetric hetero D
ChemInform Abstract: Asymmetric hetero Diels—Alder Route to Quaternary Carbon Centers: Synthesis of (-)-Malyngolide.
✍ Arun K. Ghosh; Michio Shirai 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 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

d- and l-Erythrose as sources of chiral
d- and l-Erythrose as sources of chiral quaternary carbon centers. Total synthesis of (−)-malyngolide and (+)-tanikolide
✍ Alexandros E. Koumbis; Kyriaki M. Dieti; Myrofora G. Vikentiou; John K. Gallos 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 194 KB

A highly efficient and versatile approach was applied for the total synthesis of the marine natural products (-)-malyngolide and (+)-tanikolide from isopropylidene L-and D-erythrose, using a common strategy.