Enantioselective, Organocatalytic Oxy-Michael Addition to Γ/Δ-Hydroxy-Α,β-Enones: Boronate-Amine Complexes as Chiral Hydroxide Synthons

Journal of the American Chemical Society - United States
doi 10.1021/ja076802c
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Chemical Society (ACS)

Related search

Enantioselective Synthesis of Trifluoromethylated Tertiary Thioethers Through Organocatalytic Sulfa-Michael Addition of Thiols to Β-Trifluoromethyl Β,β-Disubstituted Enones

Synthesis
Organic ChemistryCatalysis
2015English

Enantioselective Organocatalytic Amine Conjugate Addition

English

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

Chemical Communications
SurfacesAlloysMaterials ChemistryCoatingsMetalsOpticalMagnetic MaterialsFilmsCatalysisChemistryElectronicCompositesCeramics
2014English

Enantioselective Conjugate Radical Addition to A-Hydroxy Enones

English

Enantioselective Organocatalytic Double Michael Addition Reactions

English

Enantioselective Organocatalytic Approach to Α-Methylene-Δ-Lactones and Δ-Lactams

Journal of Organic Chemistry
Organic Chemistry
2008English

Enantioselective Conjugate Addition of Grignard Reagents to Enones Catalyzed by Chiral Zinc(II) Complexes

Journal of Organic Chemistry
Organic Chemistry
1990English

Organocatalytic Enantioselective Conjugate Additions to Enones

English

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

Organic and Biomolecular Chemistry
Organic ChemistryTheoretical ChemistryBiochemistryPhysical
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy