Asymmetric synthesis of. alpha.-methylene-. gamma.-butyrolactones using chiral N-monosubstituted 2-[(tributylstannyl) methyl] propenamides
K Tanaka, H Yoda, Y Isobe, A Kaji
Index: Tanaka, Kazuhiko; Yoda, Hidemi; Isobe, Yutaka; Kaji, Aritsune Journal of Organic Chemistry, 1986 , vol. 51, # 10 p. 1856 - 1866
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Citation Number: 48
Abstract
a-Methylene-y-butyrolactones were prepared in high yields on treatment of N- monosubstituted 2-[(tri-butylstannyl) methyl] propenamides with aldehydes in the presence of a Lewis acid followed by acidic hydrolysis of the resulting y-hydroxy amides. Asymmetric synthesis of a-methylene-y-butyrolactones was investigated by using a variety of chiral 24 (tributylstannyl) methyl] propenamides derived from optically active amines. Reaction of N- ...
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