553665-24-0Relevant 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
Total synthesis of microcarpalide
Gurjar, Mukund K.,Nagaprasad, Ravi,Ramana
, p. 2873 - 2875 (2007/10/03)
A total synthesis of the natural product microcarpalide is described. Ring-closing metathesis of a dienic ester was used as the key step. Mannose was used as the chiral pool material for the construction of the olefinic-acid and a Sharpless asymmetric dih
