145747-47-3

Upstream product

• 61692-28-2 1-<(Trimethylsilyl)oxy>-4-acetyl-1-cyclohexene 
• 19493-09-5 Methylenetriphenylphosphorane 
• 75-77-4 chloro-trimethyl-silane 
• 132077-84-0 (S)-(-)-1-Acetoxy-4-isopropenyl-1-cyclohexene 
• 38651-65-9 (1R,5S)-(+)-nopinone 
• 132042-13-8 (S)-(-)-1-Acetoxy-4-(1-acetoxy-1-methylethyl)-1-cyclohexene 

Downstream Products

• 22460-53-3 4-isopropenylcyclohexanone 
• 62702-87-8 (+/-)-4-isopropenyl-2-cyclohexen-1-one 
• 94597-61-2 (S)-(-)-4-isopropenyl-2-cyclohexen-1-one 

Relevant academic research and scientific papers

Efficient and convenient syntheses of (R)-(-)-cryptone and (S)-(-)-isopropenyl-2-cyclohexen-1-one

Starting with (+)-nopinone (3); (R)-(-)-cryptone (1) and (S)(-)-4-isopropenyl-2-cyclohexen-1-one (2) were synthesized in five steps and 42% overall yield, and four steps and 49% overall yield, respectively.

Substituted cycloalkylamino and cycloalkoxy heterocycles, processes for preparing them and their use as pesticides

Substituted cycloalkylamino and cycloalkoxy heterocycles, processes for preparing them and their use as pesticides The invention relates to (I) STR1 in which R1 to R5, A, X, E, U, p and n are as defined in claim 1, to processes for t

Synthetic Approach to the Amphilectane Diterpenes: The Use of Nitriles as Terminators of Carbocation-Olefin Cyclizations

A biomimetic approach to the synthesis of tricyclic terpenoid isonitriles from marine sponges is described which involves carbocation-olefin cyclization of polyolefinic precursors terminated by the stereoselective formation of a carbon-nitrogen bond.The k