160098-78-2Relevant articles and documents
First stereoselective total synthesis of cryptomoscatone D2 and syntheses of (5 R,7 S)-kurzilactone and (+)-cryptofolione by an asymmetric acetate aldol approach
Yadav, Jhillusingh,Ganganna, Bogonda,Bhunia, Dineshchandra
, p. 1365 - 1372 (2012/07/14)
An efficient concise stereoselective total synthesis of cryptomoscatone D2 and syntheses of (5R,7S)-kurzilactone and (+)-cryptofolione, based on an asymmetric acetate aldol reaction starting from trans-cinnamaldehyde, are described. The other key reaction
Total synthesis of (-)-diospongin A and (+)-cryptofolione via asymmetric aldol reaction
Kumar, Rayala Naveen,Meshram
, p. 1003 - 1007 (2011/03/21)
Stereoselective synthesis of two distinctive pyranone skeletons diospongin A and cryptofolione has been described based on an asymmetric aldol reaction starting from Chan's diene. The synthetic strategy involves the enantioselective Mukaiyama aldol, diast
Asymmetric synthesis of cryptofolione and determination of its absolute configuration
Matsuoka, Yuko,Aikawa, Kohsuke,Irie, Ryo,Katsuki, Tsutomu
, p. 187 - 194 (2007/10/03)
Two possible stereoisomers of cryptofolione, isolated from the Cryptocarya species in South Africa and Brazil, were synthesized in an enantioselective manner by using asymmetric hetero Diels-Alder reaction as the key steps. Comparative evaluation of the
