Access to Natural Valparanes and Daucanes: Enantioselective Synthesis of (−)-Valpara-2,15-diene and (+)-Isodaucene-Reference-Cited by-同舟云学术

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Access to Natural Valparanes and Daucanes: Enantioselective Synthesis of (−)-Valpara-2,15-diene and (+)-Isodaucene

Published:2019-01-02 Issue:1 Volume:82 Page:9-15
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Quílez del Moral José F.¹^ORCID,Pérez Álvaro¹,Herrador María del Mar¹,Barrero Alejandro F.¹

Affiliation:

1. Department of Organic Chemistry, Institute of Biotechnology, University of Granada, Campus Fuentenueva, 18071 Granada, Spain

Funder

Ministerio de Econom?a y Competitividad

Junta de Andalucia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.8b00129

Reference62 articles.

1. aMarcos, I. S.; Moro, R. F.; Gil-Mesón, A.; Díez, D. In Studies in Natural Products Chemistry; Rahman, A. U., Ed. Elsevier: Amsterdam, The Netherlands, 2016; Vol. 48, pp 137–207.

2. Valparene: A tricyclic diterpene hydrocarbon with a new carbon skeleton.

3. Valparane, a new diterpene skeleton (part iv). Absolute stereochemistry of valparone, valparolone and other compounds with valparane skeleton

4. Glaucolides and other constituents from south african Vernonia species

5. New Terpene Hydrocarbons from the Sponge Higginsia sp.

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