Journal of the Chemical Society. Chemical communications p. 2365 - 2366 (1994)
Update date:2022-09-26
Topics:
Tamaru, Yoshinao
Sakata, Hiroya
Kimura, Masanari
Harayama, Hiroto
Konishi, Hironobu
et al.
The thiocarbonyl group of monothiomaleimide 1 serves as a more reactive dienophile than the electron-deficient C=C double bond in the same molecule for the Diels-Alder reaction with dienes 2c-g and provides ortho-endo products 3 exclusively or predominant
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