Stereoselective synthesis of erythronolide a by extremely efficient lactonization based on conformational adjustment and high activation of seco-acid1-Reference-Cited by-同舟云学术

Stereoselective synthesis of erythronolide a by extremely efficient lactonization based on conformational adjustment and high activation of seco-acid1

Published:1990-01 Issue:13-14 Volume:46 Page:4613-4628
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Hikota Masataka,Tone Hitoshi,Horita Kiyoshi,Yonemitsu Osamu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. A Stereocontrolled Synthesis of the 16-Membered Ring Macrolide Aglycones, Niddanolide, Carbonolide B, and Platenonolide W1

2. Total synthesis of erythromycins. 5. Total synthesis of erythronolide A

3. Asymmetric total synthesis of erythromycin. 2. Synthesis of an erythronolide A lactone system

4. Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin

5. Formal total synthesis of erythromycin A. Part III. Synthesis of Woodward's carbamate key intermediate from a 1,7-dioxaspiro[5.5]undecane derivative of erythronolide A

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