913370-05-5Relevant articles and documents
An efficient asymmetric synthesis of (S)-2-cyclohexyl-2-phenylglycolic acid, the acid segment of oxybutynin
Roy, Siddharth,Sharma, Anubha,Chattopadhyay, Nilmadhav,Chattopadhyay, Subrata
, p. 7067 - 7069 (2007/10/03)
An innovative and facile synthesis of the title compound has been developed starting from (R)-cyclohexylidene glyceraldehyde. The key step in the synthesis is a chiral template-driven Grignard addition with absolute diastereocontrol. The other attractive features are the operational simplicity and the use of inexpensive compounds/reagents.
Diastereoselective Synthesis of syn-Alkanetriols from a Glyceral Derivative via K-Selectride Reduction: Application to the Synthesis of a Pheromone of the Sugarcane Weevils
Dhotare, Bhaskar,Salaskar, Avinash,Chattopadhyay, Angshuman
, p. 2571 - 2575 (2007/10/03)
K-selectride reduction of commercially available D-mannitol derived ketones 2b-i produced the corresponding alcohols 3b-i in good yields and with absolute syn-selectivity in almost all the cases. It was proposed that the bulky cyclohexylidene moiety of 3