Synthesis of the C1‘−C11‘ Oxazole-Containing Side Chain of Leucascandrolide A. Application of a Sonogashira Cross-Coupling-Reference-Cited by-同舟云学术

Synthesis of the C1‘−C11‘ Oxazole-Containing Side Chain of Leucascandrolide A. Application of a Sonogashira Cross-Coupling

Published:2002-08-22 Issue:19 Volume:67 Page:6812-6815
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dakin Les A.¹,Langille Neil F.¹,Panek James S.¹

Affiliation:

1. Department of Chemistry and Center for Streamlined Synthesis, Metcalf Center for Science and Engineering, Boston University, 590 Commonwealth Avenue, Boston, Massachusetts 02215 panek@chem.bu.edu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0204000

Reference20 articles.

1. Opposite regioselectivity in the epoxidation of geraniol and linalool with molybdenum and tungsten peroxo complexes

2. Leucascandrolide B, a New 16-Membered, Extensively Methyl-Branched Polyoxygenated Macrolide from the Calcareous SpongeLeucascandra caveolata from Northeastern Waters of New Caledonia

3. Mukaiyama Aldol−Prins Cyclization Cascade Reaction: A Formal Total Synthesis of Leucascandrolide A

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