Macrolactonizations in the Total Synthesis of Natural Products-Reference-Cited by-同舟云学术

Macrolactonizations in the Total Synthesis of Natural Products

Published:2006-01-25 Issue:3 Volume:106 Page:911-939
ISSN:0009-2665
Container-title:Chemical Reviews
language:en
Short-container-title:Chem. Rev.

Author:

Parenty A.¹,Moreau X.¹,Campagne J.-M.¹

Affiliation:

1. Institut de Chimie des Substances Naturelles, Avenue de la Terrasse, F-91198 Gif sur Yvette, France, and Ecole Nationale Supérieure de Chimie, 8 rue de l'Ecole Normale, F-34296 Montpellier, France

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cr0301402

Reference646 articles.

1. Über Lactone mit großen Ringen — die Träger des vegetabilischen Moschus‐Duftes

2. Octalactins A and B: cytotoxic eight-membered-ring lactones from a marine bacterium, Streptomyces sp

3. Structure of a novel 60-membered macrolide, quinolidomicin A1

4. Recent progress in the field of macrolide antibiotics

5. The cyclization of peptides and depsipeptides

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