37079-64-4

Upstream product

• 127-41-3 alpha-ionone 
• 127-41-3 alpha-ionone 

Downstream Products

• 67099-98-3 (3RS,4SR)-3,4-epoxy-4-((SR)-2,6,6-trimethyl-cyclohex-2-enyl)-butan-2-one-(4-phenyl semicarbazone) 
• 247171-40-0 4-hydroxy-4-(2,6,6-trimethyl-cyclohex-2-enyl)-butan-2-one 
• 97309-25-6 (Z)-4,5-Epoxy-3-methyl-5-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2-pentensaeure-methylester 
• 97309-25-6 (E)-4,5-Epoxy-3-methyl-5-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2-pentensaeure-methylester 
• 124572-59-4 α-ionone epoxyhydrazone 
• 97291-42-4 4-Methyl-6-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2H-pyran-2-on 
• 97309-31-4 trans-5-Hydroxy-4-methyl-6-(2,6,6-trimethyl-2-cyclohexen-1-yl)-5,6-dihydro-2H-pyran-2-on 
• 97309-62-1 cis-5-Chlor-4-methyl-6-(2,6,6-trimethyl-2-cyclohexen-1-yl)-5,6-dihydro-2H-pyran-2-on 
• 127-41-3 alpha-ionone 
• 57549-92-5 ⁽²⁾-1-(2,6,6-trimethylcyclohex-2-en-1-yl)butan-1-one 
• 28102-24-1 (Z)-2,6,6-Trimethyl-α-(1-propenyl)-2-cyclohexene-1-methanol 
• 139609-01-1 α-Methyl-3-(2,6,6-trimethyl-2-cyclohexen-1-yl)oxiranemethanol 
• 52610-46-5 2,6,6-Trimethyl-α-(1-propenyl)-2-cyclohexene-1-methanol 
• 139609-03-3 2-(1-Bromoethyl)-3-(2,6,6-trimethyl-2-cyclohexen-1-yl)oxirane 

Relevant academic research and scientific papers

Synthesis of the enantiomeric forms of α- and γ-damascone starting from commercial racemic α-ionone

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

Lithium naphthalenide induced reductive cleavage of α,β-epoxy ketones: An efficient procedure for the preparation of β-hydroxy ketones

Lithium naphthalenide presents itself as a mild and efficient reagent for the cleavage of α,β-epoxy ketones to give the corresponding β-hydroxy ketones in good yields.

1-Crotonyl-2,2,6-trimethylcyclohexanes

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.