Amanote Research
Register
Sign In
Highly Stereoselective Construction of Spiro[4.5]decanes by SmI2-Promoted Ketyl Radical Mediated Tandem Cyclization
doi 10.1021/ol0628255.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
FeCl3-Promoted One-Step Synthesis of Spiro[4.5]decane Derivatives
Synlett
Organic Chemistry
Construction of Bicyclic Ring Systems via a Transannular SmI2-Mediated Ketone−Olefin Cyclization Strategy
Journal of Organic Chemistry
Organic Chemistry
Cascade Radical 1,6-Addition/Cyclization of Para-Quinone Methides: Leading to Spiro[4.5]deca-6,9-Dien-8-Ones
Diastereoselective Synthesis of Optically Active C2-Substituted Spiro(4.5)decanes: Two Key Intermediates for Spirovetivane Sesquiterpenes.
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Catalytic Enantioselective Synthesis of Chiral Phthalides by SmI2-Mediated Reductive Cyclization of 2-Acylarylcarboxylates
Visible Light-Promoted Synthesis of Spiroepoxy Chromanone Derivatives via a Tandem Oxidation/Radical Cyclization/Epoxidation Process
Advanced Synthesis and Catalysis
Organic Chemistry
Catalysis
Catalytic Enantioselective Synthesis of Chiral Phthalides by SmI2-Mediated Reductive Cyclization of 2-Acylarylcarboxylates
Highly Regio- And Stereoselective Synthesis of Indene Derivatives via Electrophilic Cyclization
Development of an Additive-Controlled, SmI2-mediated Stereoselective Sequence: Telescoped Spirocyclisation, Lactone Reduction and Peterson Elimination
Beilstein Journal of Organic Chemistry
Organic Chemistry