The synthesis of quaternary carbon centers through cyclialkylations
摘要:
Treatment of conjugated dienone 1 with at strong Lewis acid at -78 degrees C produced a hydrophenanthrene with a newly created quaternary carbon. During this transformation the arene moiety becomes a dienone system. (C) 1998 Elsevier Science Ltd. All rights reserved.
The synthesis of quaternary carbon centers through cyclialkylations
摘要:
Treatment of conjugated dienone 1 with at strong Lewis acid at -78 degrees C produced a hydrophenanthrene with a newly created quaternary carbon. During this transformation the arene moiety becomes a dienone system. (C) 1998 Elsevier Science Ltd. All rights reserved.
The synthesis of quaternary carbon centers through cyclialkylations
作者:George Majetich、Jing Fang
DOI:10.1016/s0040-4039(98)01931-5
日期:1998.11
Treatment of conjugated dienone 1 with at strong Lewis acid at -78 degrees C produced a hydrophenanthrene with a newly created quaternary carbon. During this transformation the arene moiety becomes a dienone system. (C) 1998 Elsevier Science Ltd. All rights reserved.