(PDF) Mild and Metal-Free Regioselective 1,2-Addition of

Mild and Metal-Free Regioselective 1,2-Addition of Carbon Nucleophiles to Α,β-Unsaturated Imines

Synlett - Germany

doi 10.1055/s-0035-1560574

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Date

September 17, 2015

Authors

Patrice Vanelle

Cédric Spitz

Thierry Terme

Publisher

Georg Thieme Verlag KG

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Mild and Metal-Free Regioselective 1,2-Addition of Carbon Nucleophiles to Α,β-Unsaturated Imines

Synlett - Germany

doi 10.1055/s-0035-1560574

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

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Efficient Pyrrole Synthesis Using Double Nucleophilic Addition to A, B-Unsaturated Imines With Plural Nucleophiles

A Mild and Efficient Approach to Enantioenriched Α-Hydroxyethyl Α,β-Unsaturated Δ-Lactams

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Organocatalytic Michael Addition–lactonisation of Carboxylic Acids Using Α,β-Unsaturated Trichloromethyl Ketones as Α,β-Unsaturated Ester Equivalents

Regioselective Synthesis of Β-Fluoro-Α,β-Unsaturated Ketones by the Reaction of Β-Diketones With DFMBA

Enantioselective Phospha-Michael Addition of Diarylphosphines to Β,γ-Unsaturated Α-Ketoesters and Amides

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