Selectivity Control in Terpene Rearrangements: A Biomimetic Synthesis of the Halimanic Bicyclic Core
Author:
Affiliation:
1. Laboratory of Natural and Biologically Active Compounds Chemistry, Institute of Chemistry, Ministry of Education, Culture and Research
2. Laboratory of Ecological Chemistry, Institute of Chemistry, Ministry of Education, Culture and Research
Abstract
Funder
Academia de Ştiinţe a Moldovei
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0037-1610686.pdf
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1. Mollecular rearrangements in the synthesis of bioactive terpenoids with new carbon skeletons;New frontiers in natural product chemistry: A destiny on the altar of research: Dedicated to academician Pavel Vlad;2021-06
2. Asymmetric Total Synthesis of (−)-Spirochensilide A, Part 1: Diastereoselective Synthesis of the ABCD Ring and Stereoselective Total Synthesis of 13(R)-Demethyl Spirochensilide A;The Journal of Organic Chemistry;2021-01-12
3. A straightforward synthesis of natural oxygenated ent-kaurenoic acid derivatives;Synthetic Communications;2020-09-21
4. Asymmetric Total Synthesis of (−)-Spirochensilide A;Journal of the American Chemical Society;2020-04-14
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