Synthetic Studies on Hemicalide: Development of a Convergent Approach toward the C1

Synthetic Studies on Hemicalide: Development of a Convergent Approach toward the C1–C25 Fragment

Published:2013-09-03 Issue:18 Volume:15 Page:4734-4737
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Sorin Geoffroy¹,Fleury Etienne¹,Tran Christine¹,Prost Elise¹,Molinier Nicolas¹,Sautel François¹,Massiot Georges¹,Specklin Simon¹,Meyer Christophe¹,Cossy Janine¹,Lannou Marie-Isabelle¹,Ardisson Janick¹

Affiliation:

1. Faculté de Pharmacie, Université Paris Descartes, CNRS UMR 8638, 4 avenue de l’observatoire, 75270 Paris Cedex 06, France, CNRS−Pierre Fabre USR 3388, Centre de Recherche & Développement Pierre Fabre, 3 avenue Hubert Curien, 31035 Toulouse Cedex 01, France, and Laboratoire de Chimie Organique, ESPCI ParisTech, CNRS UMR 7084, 10 rue Vauquelin, 75231 Paris Cedex 05, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol402077e

Reference23 articles.

1. Marine natural products

2. Carletti, I.; Massiot, G.; Debitus, C.WO 2011/051380A1 patent, 2011.

3. Relative Stereochemical Determination and Synthesis of the C1−C17 Fragment of a New Natural Polyketide

4. Relative Stereochemical Determination and Synthesis of the C17–C25 δ-Lactone Fragment of Hemicalide

5. Assigning Stereochemistry to Single Diastereoisomers by GIAO NMR Calculation: The DP4 Probability

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