✦ LIBER ✦

Mevinic acids and analogues: preparation of a key chiral intermediate

✍ Scribed by Yuh-Lin Yang; J.R. Flack

Publisher: Elsevier Science
Year: 1982
Tongue: French
Weight: 213 KB
Volume: 23
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)85585-9

No coin nor oath required. For personal study only.

✦ Synopsis

The preparation of methyl 3-O-tert-butyldiphenylsilyl-2,4-dideoxy-B-D-erythrohexopyranoside, a key chiral intermediate for mevinic acids, and its elaboration into four mevinate analogues are described.

📜 SIMILAR VOLUMES

Synthetic transformations of the mevinic

Synthetic transformations of the mevinic acid nucleus: Preparation of a monocyclic analogue of compactin

✍ Donald S. Karanewsky 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 272 KB

Chiral synthesis of a key intermediate i

Chiral synthesis of a key intermediate in the preparation of the AF toxin IIc

✍ Mohammed Laabassi; René Grée 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 247 KB

A novel stereoselective synthesis of a c

A novel stereoselective synthesis of a chiral key intermediate for the preparation of vitamin D3

✍ Susumi Hatakeyama; Hirotoshi Numata; Seiichi Takano 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 220 KB

The preparation of a key intermediate in

The preparation of a key intermediate in the synthesis of ajaconine and atidine

✍ L.H. Zalkow; B. Kumar; D.H. Miles; J. Nabors; N. Schnautz 📂 Article 📅 1968 🏛 Elsevier Science 🌐 French ⚖ 224 KB

Preparation and conversion of chiral O-i

Preparation and conversion of chiral O-isopropylidene-protected 4-aminocyclohexenol to various key intermediates toward narcissus alkaloids

✍ Shanmugham Elango; Ying-Chuan Wang; Chien-Liang Cheng; Tu-Hsin Yan 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 73 KB

Enantiomerically pure 4-amino-5,6-O-isopropylidenedioxycyclohex-2-en-1-ol, conveniently prepared by the union of O-isopropylidenedioxycyclohexadiene with camphor-based chloronitroso ester, was employed in the synthesis of versatile key intermediates toward narcissus alkaloids.

Alternative Synthesis of 1,2,3,4-Tetrame

Alternative Synthesis of 1,2,3,4-Tetramethoxy-5-methylbenzene: A Key Intermediate for Preparing Coenzyme Q Homologues and Analogues.

✍ Jian Yang; LingLing Weng; Hu Zheng 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 21 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.