Chiral building blocks from R-(–)-carvone: N-bromosuccinimidemediated addition–sceletal rearrangement of (–)-cis-carveol
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference24 articles.
1. Synthesis of taxanes—the carvone approach; a simple, efficient stereo- and enantio-selective synthesis of the functionalised A ring
2. Bryostatin: A novel asymmetric synthesis of the C27C34 fragment starting from (R)-carvone as chiral template
3. Grob-type fragmentation of a carvone derived β-hydroxymesylate: application to the synthesis of chiral lavandulol derivatives
4. Enantiospecific Total Synthesis of (−)-Bakkenolide III and Formal Total Synthesis of (−)-Bakkenolides B, C, H, L, V, and X
5. Enantioselective synthesis of both (+)- and (−)-derivatives of bicyclo[4.3.0]nonan-8-one and -3,8-diones from R-carvone
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Solutions 251 – 300;Strategies and Solutions to Advanced Organic Reaction Mechanisms;2019
2. Antioxidant Activity of Carvone and Derivatives against Superoxide Ion;Natural Product Communications;2017-05
3. Synthesis of hydroxy derivatives of limonene;Russian Chemical Reviews;2014-04-29
4. Chiral cyclohexene block from R-(−)-carvone;Russian Journal of Organic Chemistry;2012-02
5. ChemInform Abstract: Chiral Building Blocks from R-(-)-Carvone: N-Bromosuccinimide-Mediated Addition-Skeletal Rearrangement of (-)-cis-Carveol.;ChemInform;2010-11-18
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