Anthracenic and naphthalenic vic-diepoxides. A new kind of isomerization going through fragmentation
摘要:
When treated with Lewis acids in an anhydrous medium, syn and anti anthracenic and naphthalenic vic-diepoxides 2 and 3 rearrange more or less completely to acyl-benzo, or naphthopyrans 1. This rearrangement, competing with more classical ones, appears to involve a Grob-type fragmentation followed by recyclisation. (C) 1997 Elsevier Science Ltd.
Rigaudy, Jean; Lachgar, Mohamed; Saad, Moustafa MA, Bulletin de la Societe Chimique de France, 1994, vol. 131, p. 177 - 187
作者:Rigaudy, Jean、Lachgar, Mohamed、Saad, Moustafa MA
DOI:——
日期:——
Rigaudy, Jean; Lachgar, Mohamed; Caspar, Alain, Bulletin de la Societe Chimique de France, 1996, vol. 133, # 5, p. 481 - 490
作者:Rigaudy, Jean、Lachgar, Mohamed、Caspar, Alain、Chassagnard, Claude
DOI:——
日期:——
Anthracenic and naphthalenic vic-diepoxides. A new kind of isomerization going through fragmentation
作者:Jean Rigaudy、Mohamed Lachgar
DOI:10.1016/s0040-4039(97)00294-3
日期:1997.3
When treated with Lewis acids in an anhydrous medium, syn and anti anthracenic and naphthalenic vic-diepoxides 2 and 3 rearrange more or less completely to acyl-benzo, or naphthopyrans 1. This rearrangement, competing with more classical ones, appears to involve a Grob-type fragmentation followed by recyclisation. (C) 1997 Elsevier Science Ltd.