821785-93-7Relevant academic research and scientific papers
The stereoselective total synthesis of (6S)-5,6-dihydro-6-[(2R)-2-hydroxy- 6-phenylhexyl]-2H-pyran-2-one via Prins cyclization
Yadav, Jhillu Singh,Chandrakanth, Dandekar,Rao, Yerragorla Gopala,Ravindar, Kontham,Subba Reddy, Basi V.
experimental part, p. 1432 - 1438 (2010/09/12)
The stereoselective total synthesis of an antiproliferative and antifungal a-pyrone natural product (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H- pyran-2-one is described. The key steps involved are the Prins cyclization, Mitsunobu reaction, and r
The first stereoselective total synthesis of (6S)-5,6-dihydro-6-[(2R)-2- hydroxy-6-phenylhexyl]-2H-pyran-2-one
Chandrasekhar,Narsihmulu, Ch.,Sultana, S. Shameem,Srinivasa Reddy
, p. 9299 - 9301 (2007/10/03)
Iterative asymmetric allylations and ring-closing metathesis have been effectively performed for the first stereoselective total synthesis of (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one, a novel α,β-unsaturated-δ-lactone having antifu
