Diastereocontrol in intermolecular diels-alder reactions of allenic lactones: Synthetic approach to the plaunols
摘要:
Diels-Alder cycloaddition of the allenic lactone 11 with 1-(1-(t-butyldimethylsilyloxy)vinyl)cyclohexene 6b produces the desired cycloadduct 12 with good endo selectivity (4:1) and excellent diastereoselectivity.
Diastereocontrol in intermolecular diels-alder reactions of allenic lactones: Synthetic approach to the plaunols
作者:Michael E. Jung、Craig N. Zimmerman、Gregory T. Lowen、Saeed I. Khan
DOI:10.1016/0040-4039(93)88057-p
日期:1993.7
Diels-Alder cycloaddition of the allenic lactone 11 with 1-(1-(t-butyldimethylsilyloxy)vinyl)cyclohexene 6b produces the desired cycloadduct 12 with good endo selectivity (4:1) and excellent diastereoselectivity.
Jung, Michael E.; Zimmerman, Craig N., Journal of the American Chemical Society, 1991, vol. 113, # 20, p. 7813 - 7814