Diels-alder reactions of chiral 5,5-dimethyl-4,6-methano-2-methoxycarbonyl-2-cyclohexenone
摘要:
Diels-Alder reactions of the chiral enone ester 1 proceed in high yield with addition exclusively to the less hindered Si-face to give adducts of type 5.
Liu, Hsing-Jang; Chew, Sew Yeu; Browne, Eric N. C., Canadian Journal of Chemistry, 1994, vol. 72, # 5, p. 1193 - 1210
作者:Liu, Hsing-Jang、Chew, Sew Yeu、Browne, Eric N. C.、Kim, Jeung Bea
DOI:——
日期:——
Diels-alder reactions of chiral 5,5-dimethyl-4,6-methano-2-methoxycarbonyl-2-cyclohexenone
作者:Hsing-Jang Liu、Sew Yeu Chew、Eric N.C. Browne
DOI:10.1016/s0040-4039(00)78893-9
日期:1991.4
Diels-Alder reactions of the chiral enone ester 1 proceed in high yield with addition exclusively to the less hindered Si-face to give adducts of type 5.