An efficient synthesis of o-terphenyls from Morita–Baylis–Hillman adducts of cinnamaldehydes: a consecutive bromination, Wittig reaction, 6π-electrocyclization, and an aerobic oxidation process-Reference-Cited by-同舟云学术

An efficient synthesis of o-terphenyls from Morita–Baylis–Hillman adducts of cinnamaldehydes: a consecutive bromination, Wittig reaction, 6π-electrocyclization, and an aerobic oxidation process

Published:2013-05 Issue:20 Volume:54 Page:2476-2479
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Lim Cheol Hee,Kim Sung Hwan,Kim Ko Hoon,Kim Jae Nyoung

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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3. Oxidative C−C Bond Formation (Scholl Reaction) with DDQ as an Efficient and Easily Recyclable Oxidant

4. Synthesis of Nonaphenylenes and Dodecaphenylenes Using Electron-Transfer Oxidation of Lipshutz Cuprates and Formation of Nanostructural Materials from Hexadodecyloxynonaphenylene

5. Synthesis and Characterization of Soluble Octaaryl- and Octaaryloxy-Substituted Metal-Naphthalocyanines

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