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FUNCTIONALIZATION OF 2-PHENYLSULFONYL 1,3-DIENES VIA CYCLOPROPANATION AND EPOXIDATION - SYNTHESIS OF OXABICYCLIC SYSTEMS VIA BF3-INDUCED REARRANGEMENT OF EPOXIDE DERIVATIVES
Uppsala University.
Uppsala University.
Uppsala University.
Uppsala University.
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1995 (English)In: JOURNAL OF ORGANIC CHEMISTRY, Vol. 60, no 12, 3586-3591 p.Other (Other scientific)
Abstract [en]

Regioselective cyclopropanation and epoxidation of 2-phenylsulfonyl 1,3-dienes using dimethyloxo-sulfonium methylide ((CH3)(2)SOCH2) and m-chloroperbenzoic acid (m-CPBA) gave access to 3,4-epoxy-1,2-methylene-2-phenylsulfonyl alkanes. The Lewis acid-cata

Place, publisher, year, pages
AMER CHEMICAL SOC , 1995. Vol. 60, no 12, 3586-3591 p.
Keyword [en]
DIELS-ALDER REACTIONS; ORGANIC TRANSFORMATIONS; VERSATILE SYNTHONS; CHIRAL ENAMINES; CYCLOADDITION; SULFONES; DIENES; INDOLES; ALLYL
Identifiers
URN: urn:nbn:se:uu:diva-68919OAI: oai:DiVA.org:uu-68919DiVA: diva2:96830
Note
Addresses: UNIV UPPSALA, DEPT ORGAN CHEM, S-75121 UPPSALA, SWEDEN.Available from: 2008-10-17 Created: 2008-10-17

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