Thioaldehyde Diels-Alder reactions

…, TH Eberlein, DJ Mazur, CK McClure…

Index: Vedejs, E.; Eberlein, T. H.; Mazur, D. J.; McClure, C. K.; Perry, D. A.; et al. Journal of Organic Chemistry, 1986 , vol. 51, # 9 p. 1556 - 1562

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Citation Number: 108

Abstract

Thioaldehydes containing virtually any a-substitutent can be generated by photofragmentation of phenacyl sulfides. Donor-substituted derivatives are reactive toward electron-rich dienes and give 2+ 4 cycloadducts with regiochemistry corresponding to ...

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