The first route toward oxygenated monocarbocyclic terpenoids: synthesis of elegansidiol, a new sesquiterpene from Santolina elegans-Reference-Cited by-同舟云学术

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The first route toward oxygenated monocarbocyclic terpenoids: synthesis of elegansidiol, a new sesquiterpene from Santolina elegans

Published:1999-11 Issue:47 Volume:40 Page:8273-8276
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Barrero Alejandro F.,Alvarez-Manzaneda Enrique J.,Mar Herrador M.,Alvarez-Manzaneda R.,Quilez J.,Chahboun R.,Linares P.,Rivas A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference5 articles.

1. Achilleol A: A new monocyclic triterpene skeleton from Achillea odorata L.

2. The Biogenetically Patterned in vitro Oxidation-Cyclization of Farnesyl Acetate

3. Marine brown algae of family Cystoseiraceae: Chemistry and chemotaxonomy

4. Synthesis of (±)-karahana ether and karahanaenone by selective cyclization of 6,7-epoxygeranyl acetate

5. Synthesis of (±)-karahana ether and a (±)-labdadienoic acid by the electrophilic cyclization of epoxy allylsilanes

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2. A Review of the Traditional Uses, Phytochemistry and Biological Activities of the Genus Santolina;Planta Medica;2018-03-08

3. Enantioselective Syntheses of the Proposed Structures of Kopeolin and Kopeolone;Chemistry - A European Journal;2013-06-27

4. Protein engineering of oxidosqualene-lanosterol cyclase into triterpene monocyclase;Organic & Biomolecular Chemistry;2013

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