Synthesis of fused chromene-1,4-naphthoquinones via ring-closing metathesis and Knoevenagel-electrocyclization under acid catalysis and microwave irradiation-Reference-Cited by-同舟云学术

Synthesis of fused chromene-1,4-naphthoquinones via ring-closing metathesis and Knoevenagel-electrocyclization under acid catalysis and microwave irradiation

Published:2014-05 Issue:20 Volume:70 Page:3266-3270
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

da Rocha David R.,Mota Kelly,da Silva Illana M.C.B.,Ferreira Vitor F.,Ferreira Sabrina B.,da Silva Fernando de C.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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2. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure–activity relationships of the 7- and 5-, 6-, 8-positions

3. A novel QSAR model for predicting induction of apoptosis by 4-aryl-4H-chromenes

4. Stereoselective syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogues

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