✦ LIBER ✦

Synthesis of macrolide antibiotics. 3. Revised synthesis of C9- C13 segment of erythronolide A.

✍ Scribed by N.K. Kochetkov; A.F. Sviridov; M.S. Ermolenko; D.V. Yashunsky

Publisher: Elsevier Science
Year: 1984
Tongue: French
Weight: 210 KB
Volume: 25
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)90023-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of macrolide antibiotics. 2. S

Synthesis of macrolide antibiotics. 2. Synthesis of the C9-C13 segments of erythronolides A, B and oleandonolide

✍ N.K. Kochetkov; A.F. Sviridov; M.S. Ermolenko; N.D. Zelinsky 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 234 KB

The Cg-C,3 segments of some l+membered macrolide antibiotics have

Synthesis of macrolide antibiotics. 1. S

Synthesis of macrolide antibiotics. 1. Synthesis of the C1-C6 segment of 14-membered macrolide antibiotics.

✍ N.K. Kochetkov; A.F. Sviridov; M.S. Ermolenko; N.D. Zelinsky 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 221 KB

The C,-C6 segment of a number of 14-membered macrolide antibiotics have been synthesized started from levoglucosan.

Studies in macrolide synthesis: Stereoco

Studies in macrolide synthesis: Stereocontrolled synthesis of a C1C13 segment of concanamycin A

✍ Ian Paterson; Malcolm D. McLeod 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 329 KB

The Ct-Ct3 segment 6 of concanamycin A (1) was prepared by a highly stereocontrolled route (87% overall ds) in 16 steps from the ester 9. Key steps are the one-pot aldol/reduction, 8 + 12, and the HWB reaction, 18 + 19 + 6.8 1997 Elsevier Science Ltd.

ChemInform Abstract: Studies in Macrolid

ChemInform Abstract: Studies in Macrolide Synthesis: Stereocontrolled Synthesis of a C1-C13 Segment of Concanamycin A.

✍ I. PATERSON; M. D. MCLEOD 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 views

An Enantioselective Synthesis of the C1—

An Enantioselective Synthesis of the C1—C9 Segment of Antitumor Macrolide Peloruside A.

✍ Arun K. Ghosh; Jae-Hun Kim 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 238 KB 👁 2 views

An enantioselective synthesis of the C1

An enantioselective synthesis of the C1C9 segment of antitumor macrolide peloruside A

✍ Arun K. Ghosh; Jae-Hun Kim 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 174 KB

A stereocontrolled synthesis of the C 1 C 9 segment of the marine natural product peloruside A is described. The key steps involve Sharpless's catalytic asymmetric dihydroxylation reaction, a chelation-controlled reduction of chiral b-alkoxy ketones to elaborate the syn-1,3-diol functionality and a