作者:Christiane Santelli-Rouvier、Sophie Lefrère、Maurice Santelli
DOI:10.1016/0040-4039(94)88086-7
日期:1994.8
pentanones followed by dehydration, 1,4-reduction of the triene, ozonolysis and Baeyer-Villiger oxidation afforded a δ-lactone (28 % of overall yield), well-known precursor of the Prelog-Djerassi Lactone.
将巴豆基格氏试剂立体选择性加入2-亚烷基-5-甲基环戊酮中,然后脱水,三烯进行1,4-还原,臭氧分解和Baeyer-Villiger氧化,得到了δ-内酯(占总收率的28%) Prelog-Djerassi内酯的前体。