Synthesis of optically active 1-t-butyl-4-ethylidenecyclohexane via CO2-elimination from a spirofused β-lactone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
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3. Enantioselective catalytic isomerization of an unfunctionalized achiral alkene
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1. Formation of Alkenes by Elimination;Comprehensive Organic Transformations;2018-02-28
2. Construction of Successive Chiral Centers Adjacent to a Chiral Tetraalkylated Quaternary Center Using an Asymmetric Aldol Reaction;Organic Letters;2013-04-11
3. Reversal of Selectivity in Acetate Aldol Reactions of N-Acetyl-(S)-4-isopropyl-1-[(R)-1-phenylethyl]imidazolidin-2-one;Organic Letters;2012-05-09
4. Cyclopropanespiro-β-lactones derived from 4-[(Z)-ethylidene]-3-methyloxetan-2-one: diastereoselective formation and rearrangement reactions;Tetrahedron;2011-05
5. ChemInform Abstract: Synthesis of Optically Active 1-t-Butyl-4-ethylidenecyclohexane via CO2-Elimination from a Spirofused β-Lactone.;ChemInform;2010-08-12
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