1-Hydroxy-7-methylene bicyclo[3.2.1]octane: a gibbane-steviol c/d ring model
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. A New Cyclization. 2-Methylenecyclopentanols by the Chemical Reduction of γ-Ethinyl Ketones
2. Studies on the Total Synthesis of Gibberellic Acids. A Simple Route to the Tetracarbocyclic Network
3. A new method for the construction of a bicyclo[3.2.1]octane ring system with a bridgehead hydroxyl group - a partial synthesis of (−)-epiallogibberic acid
4. Total synthesis of (±)-steviol
5. A synthesis of steviol
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1. Dearomative logic in natural product total synthesis;Natural Product Reports;2022
2. Scalable synthesis enabling multilevel bio-evaluations of natural products for discovery of lead compounds;Nature Communications;2018-03-29
3. Convergent Route to ent-Kaurane Diterpenoids: Total Synthesis of Lungshengenin D and 1α,6α-Diacetoxy-ent-kaura-9(11),16-dien-12,15-dione;Journal of the American Chemical Society;2017-02-14
4. Chemistry and Bioactivity of ent -Kaurene Diterpenoids;Studies in Natural Products Chemistry;2017
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