An expedient synthesis of poly-substituted naphthalenes: consecutive Michael, intramolecular aldol, and decarboxylative Michael cascade of δ-ketonitriles-Reference-Cited by-同舟云学术

An expedient synthesis of poly-substituted naphthalenes: consecutive Michael, intramolecular aldol, and decarboxylative Michael cascade of δ-ketonitriles

Published:2010-03 Issue:12 Volume:51 Page:1592-1595
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kim Sung Hwan,Kim Yu Mi,Lee Hyun Seung,Kim Jae Nyoung

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Regioselective synthesis of 1-arylnaphthalenes from N-tosylaziridine derivatives

2. One-Pot Synthesis of Naphthalenes from Baylis-Hillman Adducts via Pd-Mediated Successive Allylation and Arylation

3. Synthesis of 1,3-disubstituted naphthalenes from the Baylis–Hillman acetates with the aid of manganese(III) acetate

4. Radical cyclization of 4-aryl-1-iodobutene derivatives to form dihydronaphthalene scaffold

5. Synthesis of Naphthalenes from the Reaction of Baylis-Hillman Acetates and Sulfonyl Group-containing Active Methylene Compounds

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