Asymmetric Total Synthesis of ent-(−)-Roseophilin: Assignment of Absolute Configuration-Reference-Cited by-同舟云学术

Asymmetric Total Synthesis of ent-(−)-Roseophilin: Assignment of Absolute Configuration

Published:2001-08-10 Issue:35 Volume:123 Page:8515-8519
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Boger Dale L.¹,Hong Jiyong¹

Affiliation:

1. Contribution from the Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja011271s

Reference53 articles.

1. Structure of a new antibiotic, roseophilin

2. Synthesis of various model compounds for the conjugated heterocyclic ring system of antibiotic roseophilin

3. Conversion of δ-(sulfonyl)amino-α-epoxy ketones to bicyclic ketopyrroles via intramolecular conjugate-addition to azoene intermediates. Synthesis of the bicyclic ketopyrrole core of the 1-azafulvene roseophllin

4. Total Synthesis of the Potent Antitumor Agent Roseophilin: A Concise Approach to the Macrotricyclic Core

5. Application of the grubbs ring-closing metathesis for the construction of a macrocyclic ansa-bridge. Synthesis of the tricyclic core of roseophilin

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