Miyata O, Nakajima E, Naito T
Kobe Pharmaceutical University, Higashinada, Japan.
Chem Pharm Bull (Tokyo). 2001 Feb;49(2):213-24. doi: 10.1248/cpb.49.213.
Sulfanyl radical addition-addition-cyclization (SRAAC) of unbranched diynes proceeded smoothly to give cyclized exo-olefins, while the sulfanyl radical addition-cyclization-addition (SRACA) of diynes having a quaternary carbon gave cyclized endo-olefins. This method was successfully applied to the synthesis of A-ring fragment of 1alpha,25-dihydroxyvitamin D3.
直链二炔的硫烷基自由基加成-加成-环化(SRAAC)反应顺利进行,生成环化的外向烯烃,而具有季碳的二炔的硫烷基自由基加成-环化-加成(SRACA)反应则生成环化的内向烯烃。该方法成功应用于1α,25-二羟基维生素D3 A环片段的合成。