Methoxymercurierung von bullvalen und bicyclo[4.2.2]deca-2,4,7,9-tetraen
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Moleküle mit schneller und reversibler Valenzisomerisierung, VI. Synthesen und Eigenschaften einiger monosubstituierter Bullvalene
2. Fluor-, chlor- und jodbullvalen
3. Unsaturated heterocyclic systems. LIX. Competitive 1,2- and 1,6-cycloadditions to bullvalene
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1. Reactions of functionally substituted bicyclo[4.2.2]deca-2,4,7,9-tetraenes with m-chloroperbenzoic acid and in vitro evaluation Of Product Cytotoxicity against tumor cells;Mendeleev Communications;2019-09
2. 1,4-Pentadienyl-3-sulfonamides: Frameworks for “Disfavored” Radical Cascade Cyclizations;Organic Letters;2001-09-12
3. Radical Cyclizations by Intramolecular Additions;Reactive Intermediates;1982
4. 1,2-ARYL MIGRATION AND EXPERIMENTAL EVIDENCE FOR A TWO-STEP MECHANISM IN THE ELECTROPHILIC ADDITION OF BENZENESULFENYL CHLORIDE TO OLEFINIC SYSTEMS;Phosphorus and Sulfur and the Related Elements;1977-04
5. Skeletal rearrangement in the methoxymercuration of 2-methyl-3-arylbut-1-ene-3-ols;Journal of Organometallic Chemistry;1974-12
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