Enantioselective synthesis of spiro[4.5]decanone with 2-(S)-methoxy-1,4-dibromobutane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Spiroannelation of enol ethers of cyclic 1,3-diketones. Simple stereospecific synthesis of .beta.-vetivone
2. A Facile Synthesis of (−)-β-Vetivone
3. An asymmetric total synthesis of fragrant spiro[4.5]decane sesquiterpene (-)-.beta.-vetivone via an enantiomerically pure vinylic sulfoxide
4. Structure and synthesis of .beta.-vetivone
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1. Alkylation and Acylation of Aldehydes, Ketones, and Their Derivatives;Comprehensive Organic Transformations;2018-02-28
2. Formation of Alcohols and Phenols by Alkylation of Carbonyl Compounds;Comprehensive Organic Transformations;2018-02-28
3. Cationic Cyclization of 2-Alkenyl-1,3-dithiolanes: Diastereoselective Synthesis of trans-Decalins;The Journal of Organic Chemistry;2011-04-13
4. An efficient one-pot four-step domino reaction for the synthesis of C2-substituted 3-methylcyclohex-2-enones;Tetrahedron;2010-09
5. ChemInform Abstract: Enantioselective Synthesis of Spiro(4.5)decanone with 2-(S)-Methoxy-1, 4-dibromobutane.;ChemInform;2010-08-19
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