Stereoselective Pd-catalyzed etherification and asymmetric synthesis of furanomycin and its analogues from a chiral aziridine-Reference-Cited by-同舟云学术

Stereoselective Pd-catalyzed etherification and asymmetric synthesis of furanomycin and its analogues from a chiral aziridine

Published:2015 Issue:30 Volume:13 Page:8187-8195
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Jung Jae-Hoon¹²³⁴⁵,Yoon Doo-Ha¹²³⁴⁵,Lee Kyuwoong²⁶⁷⁵,Shin Hyeonah²⁶⁷⁵,Lee Won Koo²⁶⁷⁵,Yook Cheol-Min¹²³⁴⁵,Ha Hyun-Joon¹²³⁴⁵

Affiliation:

1. Centre for new Directions in Organic Synthesis

2. Department of Chemistry

3. Hankuk University of Foreign Studies

4. Yongin, Kyunggi-Do

5. Korea

6. Sogang University

7. Seoul 121-742

Abstract

A chiral aziridine was utilized for the synthesis of the anti-bacterial natural amino acidl-(+)-furanomycin, and its analogues including 5′-epi-furanomycin and norfuranomycin.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB00375J

Reference52 articles.

1. Synthesis ofL-Furanomycin and Its Analogues via Furoisoxazolines

2. Straightforward Syntheses of Furanomycin Derivatives and their Biological Evaluation

3. A New Antibiotic. Furanomycin, an Isoleucine Antagonist

4. X-Ray crystal structure determination of furanomycin

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