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 = 다중치환된 나프탈렌의 선택적 합성
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- Title
- 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 = 다중치환된 나프탈렌의 선택적 합성
- Author(s)
- S H Kim; Sangku Lee; H S Lee; J N Kim
- Bibliographic Citation
- Tetrahedron Letters, vol. 51, no. 48, pp. 6305-6309
- Publication Year
- 2010
- Abstract
- 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 reaction and an aerobic oxidation process.
- Keyword
- 6-endo Heck reactionBaylis-Hillman adductsNaphthalenesPalladium
- ISSN
- 0040-4039
- Publisher
- Elsevier
- Full Text Link
- http://dx.doi.org/10.1016/j.tetlet.2010.09.127
- Type
- Article
- Appears in Collections:
- Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
- Files in This Item:
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