Reductive C–C Bond Formation after Epoxide Opening via Electron Transfer
- 9 May 2007
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 118 references indexed in Scilit:
- Titanocene‐Mediated Radical Cyclization: An Emergent Method Towards the Synthesis of Natural ProductsEuropean Journal of Organic Chemistry, 2006
- A Combined Theoretical and Experimental Study of Efficient and Fast Titanocene-Catalyzed3-exoCyclizationsJournal of the American Chemical Society, 2005
- Influence of the Halogen in Titanocene Halide Promoted ReductionsOrganometallics, 2005
- Mechanistic Investigation of the Electrochemical Reduction of Cp2TiX2Organometallics, 2004
- The Effect of Open and Closed Structures of Titanocenes on the Control of Diastereoselectivity of Radical ReactionsOrganometallics, 2004
- Stereospecific Synthesis of Polyfunctionalized Carbacephams Induced by Titanocene(III) ChlorideThe Journal of Organic Chemistry, 2003
- Stereospecific Synthesis of Highly Functionalized Tricyclic β-Lactams by Radical Cyclizations Using Titanocene MonochlorideThe Journal of Organic Chemistry, 2002
- Titanium(IV) Aryloxide Catalyzed Cyclization Reactions of 1,6- and 1,7-DienesJournal of the American Chemical Society, 2000
- Emergence of a Novel Catalytic Radical Reaction: Titanocene-Catalyzed Reductive Opening of EpoxidesJournal of the American Chemical Society, 1998
- Catalytic, Highly Regio- and Chemoselective Generation of Radicals from Epoxides: Titanocene Dichloride as an Electron Transfer Catalyst in Transition Metal Catalyzed Radical ReactionsAngewandte Chemie International Edition, 1998