Efficient one-pot synthesis of benzopyranobenzopyrans and naphthopyranobenzopyrans by domino aldol-type reaction/hetero Diels–Alder reaction of resorcinols and naphthols-Reference-Cited by-同舟云学术

Efficient one-pot synthesis of benzopyranobenzopyrans and naphthopyranobenzopyrans by domino aldol-type reaction/hetero Diels–Alder reaction of resorcinols and naphthols

Published:2009-01 Issue:1 Volume:65 Page:101-108
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Lee Yong Rok,Kim Yun Mi,Kim Sung Hong

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference72 articles.

1. Efficient Asymmetric Synthesis of 2,6‐Disubstituted 2 H ‐Dihydropyrans via a Catalytic Hetero‐Diels–Alder/Allylboration Sequence

2. [4+2] Cycloaddition ofortho-Quinone Methides Promoted by Ionic Liquids: an Efficient and Mild Protocol for the Synthesis of Tetrahydropyranobenzopyrans

3. Ethylene-Bridged Bissulfoximines in Copper-Catalyzed Enantioselective Hetero-Diels--Alder Reactions

4. Chiral Chromium(III) Porphyrins as Highly Enantioselective Catalysts for Hetero-Diels–Alder Reactions Between Aldehydes and Dienes

5. Proline-Catalyzed Imino-Diels–Alder Reactions: Synthesis ofmeso-2,6-Diaryl-4-piperidones

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