1039357-66-8Relevant academic research and scientific papers
A chemoenzymatic synthesis of hept-6-ene-2,5-diol stereomers: Application to asymmetric synthesis of decarestrictine L, pyrenophorol, and stagonolide e
Chatterjee, Sucheta,Ghadigaonkar, Sneha,Sur, Payel,Sharma, Anubha,Chattopadhyay, Subrata
, p. 8067 - 8076 (2015/03/18)
The stereomers of hept-6-ene-2,5-diol derivatives were conceived as useful chiral intermediates and were synthesized starting from sulcatol using two lipase-catalyzed acylation reactions as the key steps. The versatility of the intermediates was demonstrated by converting them to the titled tetrahydropyran, macrolide, and macrodiolide compounds using standard synthetic protocols.
Facile total synthesis of the antimalarial nonenolide
Liu, Jian,Zhang, Ling,He, Jinmei,He, Liuer,Ma, Bowen,Pan, Xinfu,She, Xuegong
, p. 906 - 911 (2008/09/21)
The facile total synthesis of the antimalarial nonenolide 1 is reported. The convergent strategy features the use of reactions such as Sharpless asymmetric dihydroxylation, aldol addition, Mitsunobu reaction, and ring-closing metathesis (RCM).
