Diels–Alder intramolecular cycloaddition of vinylallenyl cycloalken-3-yl ethers
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1993/C3/C39930000270
Reference19 articles.
1. Synthesis of the hexahydronaphthalene moiety of (.+-.)-compactin (ML-236B)
2. Novel bicycloannulation via tandem vinylation and intramolecular Diels-Alder reaction of five-membered heterocycles: a new approach to construction of psoralen and azapsoralen
3. Competitive intramolecular [4 + 2] cycloaddition and tandem [2 + 2] cycloaddition/ [3,3]-sigmatropic rearrangement sequence of allenyl 3-vinyl-2-cyclohexenyl ethers: evidence for switching of the reaction pathway by the substituent effects
4. Base-catalysed intramolecular cycloadditions of allyl 3-phenylprop-2-ynyl ethers and 4-methylpent-4-en-2-ynyl prop-2-ynyl ethers
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1. Branching out: redox strategies towards the synthesis of acyclic α-tertiary ethers;Chemical Society Reviews;2022
2. Allenes in Diels–Alder Cycloadditions;Synthesis;2021-08-04
3. Regio- and stereoselective Diels-Alder reaction of diphenyl 5-methylhexa-1,3,4-trien-3-yl phosphine oxide with N-(4-substituted-phenyl)maleimides and maleic anhydride;Arkivoc;2013-08-18
4. The chemistry of bisallenes;Beilstein Journal of Organic Chemistry;2012-11-15
5. An Effective Diels-Alder Reaction of Vinyl Allenols with Dienophiles;European Journal of Organic Chemistry;2011-01-12
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