A [2++4] polar cycloaddition of α-chlorosulfides with conjugated dienes: one-pot synthesis of 1-acyl- and 1-cyano-1-methylthio-2-vinylcyclopropanes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Cationic polar cycloaddition with chloromethyl phenyl sulfides
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4. Polar cycloaddition of α-acyl-α-chlorosulfides with alkynes. Novel one-step syntheses of furans and 2-furanones
5. Reaction of 1,3-dithienium fluoroborate with 1,3-dienes. Synthesis of .DELTA.3-cyclopenten-1-ones
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1. Ring Contraction of 3,6-Dihydro-2H-thiopyrans to Thiolanes by an Iodo-Oxyacylation Reaction;European Journal of Organic Chemistry;2004-01
2. A novel tandem [4++2] cycloaddition–elimination reaction: 2-alkenyl-4,4-dimethyl-1,3-oxathianes as synthetic equivalents for α,β-unsaturated thioaldehydes;Tetrahedron;2003-03
3. A novel tandem [4++2] cycloaddition–elimination reaction of 4,4-dimethyl-2-styryl-1,3-oxathianes with olefins;Tetrahedron Letters;2000-01
4. Alkylation and annulation of 3-(phenylsulfonyl)-2-alkyl-2,3-dihydroisoindol-1-ones;Tetrahedron Letters;1998-04
5. Pummerer reaction of 2-vinylcyclopropyl sulfoxides: generation and reactions of butadienylthionium ion intermediates;Journal of the Chemical Society, Perkin Transactions 1;1998
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