37079-64-4Relevant articles and documents
Synthesis of the enantiomeric forms of α- and γ-damascone starting from commercial racemic α-ionone
Serra, Stefano,Fuganti, Claudio
, p. 1573 - 1580 (2007/10/03)
A straightforward synthesis of both enantiomers of α- and γ-damascone is described. The title compounds were prepared by a divergent pathway starting from the enantiomeric forms of (6RS,7SR,9RS)-7-hydroxy-7,8-dihydro-α-ionol and of (6RS,7SR,9RS)-7-hydroxy
Olefin epoxidations using the dicyclohexylcarbodiimide - H2O2 system
Murray, Robert W.,Iyanar, Kaliappan
, p. 1730 - 1731 (2007/10/03)
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1-Crotonyl-2,2,6-trimethylcyclohexanes
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, (2008/06/13)
1-CROTONOYL-2,2,6-TRIMETHYLCYCLOHEXANE OCCURS IN FOUR STEREOISOMERIC FORMS. In particular the trans, E isomer has interesting organoleptic properties and is useful in the preparation of perfume and flavoring compositions. Processes for preparing the stereoisomers, in a pure form or as mixtures, are described.