Amanote Research

Amanote Research

    RegisterSign In

Amino Alcohols as Ligands for Nickel-Catalyzed Suzuki Reactions of Unactivated Alkyl Halides, Including Secondary Alkyl Chlorides, With Arylboronic Acids

doi 10.1021/ja0613761.s001
Full Text
Open PDF
Abstract

Available in full text

Date

Unknown

Authors

Unknown

Publisher

American Chemical Society (ACS)


Related search

Alkyl—Alkyl Suzuki Cross-Couplings of Unactivated Secondary Alkyl Halides at Room Temperature.

ChemInform
2007English

Ni-Catalyzed Carboxylation of Unactivated Alkyl Chlorides With CO2

English

Ni-Catalyzed Carboxylation of Unactivated Alkyl Chlorides With CO2

English

Photoinduced, Copper-Catalyzed Alkylation of Amides With Unactivated Secondary Alkyl Halides at Room Temperature

Journal of the American Chemical Society
BiochemistryColloidCatalysisChemistrySurface Chemistry
2014English

Nickel-Catalyzed Coupling of Alkyl Halides and Alkyl Grignard Reagents

Synfacts
2009English

Nickel-Catalyzed Diastereoselective Alkyl–Alkyl Kumada Coupling Reactions

Organic Letters
BiochemistryOrganic ChemistryTheoretical ChemistryPhysical
2012English

Nickel-Catalyzed Reductive Amidation of Unactivated Alkyl Bromides

Angewandte Chemie - International Edition
CatalysisChemistry
2016English

Silver-Catalyzed Coupling Reactions of Alkyl Halides With Indenyllithiums

Tetrahedron
Organic ChemistryBiochemistryDrug Discovery
2010English

Nickel-Catalyzed Formal Aminocarbonylation of Unactivated Alkyl Iodides With Isocyanides

English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy