Enantioselective Synthesis of Herbertane Sesquiterpenes. Synthesis of (−)-Herbertene and (−)-α-Herbertenol
Author:
Affiliation:
1. Departamento de Química Orgánica, Facultad de Químicas, Universidad de Valencia, C/Dr. Moliner 50, E-46100 Burjassot, Valencia, Spain
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo982020d
Reference13 articles.
1. Connolly, J. D.; Hill, R. A. InDictionary of Terpenoids, 1st ed.; Chapman and Hall: London, 1991; Vol. 1, pp 299−300. Also see: Fraga, B. M.Nat. Prod.Rep.1992,9, 217;1993,10, 397;1994,11, 533;1995,12, 303;1996,13, 307;1997,14, 145;1998,15, 73.
2. Structures of ent-herbertane sesquiterpenoids displaying antifungal properties from the liverwort Herberta adunca
3. Novel neurotrophic isocuparane-type sesquiterpene dimers, mastigophorenes A, B, C and D, isolated from the liverwort Mastigophora diclados
4. Total synthesis of herbertenediol, an isocuparane sesquiterpene isolated from liverworts
5. A Simple Enantioselective Synthesis of (-)-S- and (+)-R-Camphonanic Acids
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