Regioselective synthesis of poly-substituted naphthalenes via a Pd-catalyzed cyclization of modified Baylis-Hillman adducts: Selective 6-endo Heck reaction and an aerobic oxidation cascade
Poly-substituted naphthalenes were synthesized via a Pd-catalyzed cyclization of modified Baylis-Hillman adducts having an o-bromophenyl acetonitrile moiety at the secondary position, in reasonable yields. The reaction involved a sequential 6-endo Heck re
Kim, Se Hee,Lee, Sangku,Lee, Hyun Seung,Kim, Jae Nyoung
scheme or table
p. 6305 - 6309
(2011/01/04)
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