852509-25-2Relevant academic research and scientific papers
Enantiodivergent total synthesis of microcarpalide from l-tartaric acid
Prasad, Kavirayani R.,Penchalaiah, Kamala
, p. 4268 - 4276 (2011/06/26)
Stereoselective approach for the synthesis of both enantiomers of bio-active decanolactone microcarpalide is described from l-tartaric acid. The synthesis of the key intermediates en route to the natural product is achieved from l-tartaric acid involving
Stereoselective synthesis of (-)-microcarpalide
Prasad, Kavirayani R.,Penchalaiah, Kamala,Choudhary, Amit,Anbarasan, Pazhamalai
, p. 309 - 311 (2007/10/03)
A stereoselective approach for the synthesis of the bio-active decanolactone (-)-microcarpalide was achieved from chiral pool tartaric acid. The synthesis of pivotal intermediates en route to the decanolactone was achieved from α-benzyloxy aldehydes deriv
Enantioselective total synthesis of (-)-microcarpalide
Davoli, Paolo,Fava, Raffaele,Morandi, Stefania,Spaggiari, Alberto,Prati, Fabio
, p. 4427 - 4436 (2007/10/03)
The enantioselective total synthesis of the actin-targeting metabolite (-)-microcarpalide is described. Key steps include ring-closing metathesis (RCM) for the final construction of the 10-membered lactone framework and stereoselective homologation of bor
