Regioselective cyclopropanation via unsymmetrical oxatrimethylenemethane palladium intermediates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. [3+2] Cycloaddition Approaches to Five-Membered Rings via Trimethylenemethane and Its Equivalents [New Synthetic Methods (55)]
2. Criteria for concertedness in cycloadditions
3. Cyclopropenes and methylenecylopropanes as multifunctional reagents in transition metal catalyzed reactions
4. On an (oxatrimethylenemethane)palladium(0) complex. An unusual palladium(0)-catalyzed cyclopropanation
5. Chemistry of metallacyclobutanones. Part 2. Synthesis and ring inversion of some highly puckered metallacyclobutan-3-one (slipped oxodimethylenemethane) complexes of palladium; crystal structures of 2,4-bis(methoxycarbonyl)-1,1-bis(triphenylphosphine)palladacyclobutan-3-one, 2,4-bis(methoxycarbonyl)-1,1-bis(triphenylarsine)palladacyclobutan-3-one, and 1,1-(2′,2″-bipyridyl)-2,4-bis(methoxycarbonyl)palladacyclobutan-3-one
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