Sequential ring-closing enyne metathesis and intramolecular Diels–Alder reaction: an approach to the synthesis of the core structure of galiellalactone-Reference-Cited by-同舟云学术

Sequential ring-closing enyne metathesis and intramolecular Diels–Alder reaction: an approach to the synthesis of the core structure of galiellalactone

Published:2020-10-31 Issue:1 Volume:132 Page:
ISSN:0974-3626
Container-title:Journal of Chemical Sciences
language:en
Short-container-title:J Chem Sci

Author:

Datta Ritabrata,Ghosh Subrata^ORCID

Funder

Indian National Science Academy

Council of Scientific and Industrial Research, India

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s12039-020-01842-w.pdf

Reference17 articles.

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2. Johansson M, Kopcke B, Anke H and Sterner O 2002 Cyclization of (-)-pregaliellalactone in the fungus Galiellarufa Angew. Chem. Int. Ed. 41 2158

3. Johansson M and Sterner O 2001 Synthesis of (+)-galiellalactone. Absolute configuration of galiellalactone Org. Lett. 19 2843

4. Johansson M, Köpcke B, Anke H and Sterner O 2002 Synthesis of (-)-pregaliellalactone, conversion of (-)-pregaliellalactone to (-)-galiellalactone by mycelia of Galiellarufa Tetrahedron 58 2523

5. Lebel H and Parmentier M 2007 Copper-catalyzed methylenation reaction: Total synthesis of (+)-desoxygaliellalactone Org. Lett. 9 3563

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