Anti-Markovnikov intermolecular hydroamination of alkenes and alkynes: a mechanistic view
Hydroamination, the addition of an N–H bond across a C–C multiple bond, is a reaction with
a great synthetic potential. Important advances have been made in the last decades …
a great synthetic potential. Important advances have been made in the last decades …
Alkaline earths as main group reagents in molecular catalysis
The past decade has witnessed some remarkable advances in our appreciation of the
structural and reaction chemistry of the heavier alkaline earth (Ae= Mg, Ca, Sr, Ba) elements …
structural and reaction chemistry of the heavier alkaline earth (Ae= Mg, Ca, Sr, Ba) elements …
From limestone to catalysis: application of calcium compounds as homogeneous catalysts
S Harder - Chemical reviews, 2010 - ACS Publications
Organometallic chemistry is generally considered the key to homogeneous catalysis, which,
although a century old, is still today a very dynamic discipline. 1 The past decade has seen …
although a century old, is still today a very dynamic discipline. 1 The past decade has seen …
anti‐Markovnikov Hydroamination of Alkenes Catalyzed by a Two‐Component Organic Photoredox System: Direct Access to Phenethylamine Derivatives
TM Nguyen, N Manohar… - Angewandte Chemie …, 2014 - Wiley Online Library
Disclosed herein is a general catalytic system for the intermolecular anti‐Markovnikov
hydroamination of alkenes. By using an organocatalytic photoredox system, α‐and β …
hydroamination of alkenes. By using an organocatalytic photoredox system, α‐and β …
Enantioselective CuH-catalyzed anti-Markovnikov hydroamination of 1, 1-disubstituted alkenes
S Zhu, SL Buchwald - Journal of the American Chemical Society, 2014 - ACS Publications
Enantioselective synthesis of β-chiral amines has been achieved via copper-catalyzed
hydroamination of 1, 1-disubstituted alkenes with hydroxylamine esters in the presence of a …
hydroamination of 1, 1-disubstituted alkenes with hydroxylamine esters in the presence of a …
The chemistry of univalent metal β-diketiminates
YC Tsai - Coordination Chemistry Reviews, 2012 - Elsevier
The easily electronically and sterically tunable β-diketiminates are widely used auxiliary
ligands for the creation of a wide range of metal complexes with various oxidation states in …
ligands for the creation of a wide range of metal complexes with various oxidation states in …
[图书][B] Early main group metal catalysis: concepts and reactions
S Harder - 2019 - books.google.com
Early Main Group Metal Catalysis gives a comprehensive overview of catalytic reactions in
the presence of group 1 and group 2 metals. Chapters are ordered to reaction type, contain …
the presence of group 1 and group 2 metals. Chapters are ordered to reaction type, contain …
Heterofunctionalization catalysis with organometallic complexes of calcium, strontium and barium
AGM Barrett, MR Crimmin, MS Hill… - Proceedings of the …, 2010 - royalsocietypublishing.org
Despite the routine employment of Grignard reagents and Hauser bases as stoichiometric
carbanion reagents in organic and inorganic synthesis, a defined reaction chemistry …
carbanion reagents in organic and inorganic synthesis, a defined reaction chemistry …
Heavier alkaline earth catalysts for the intermolecular hydroamination of vinylarenes, dienes, and alkynes
C Brinkmann, AGM Barrett, MS Hill… - Journal of the …, 2012 - ACS Publications
The heavier group 2 complexes [M {N (SiMe3) 2} 2] 2 (1, M= Ca; 2, M= Sr) and [M {CH
(SiMe3) 2} 2 (THF) 2](3, M= Ca; 4, M= Sr) are shown to be effective precatalysts for the …
(SiMe3) 2} 2 (THF) 2](3, M= Ca; 4, M= Sr) are shown to be effective precatalysts for the …
Main group bimetallic partnerships for cooperative catalysis
JM Gil-Negrete, E Hevia - Chemical Science, 2021 - pubs.rsc.org
Over the past decade s-block metal catalysis has undergone a transformation from being an
esoteric curiosity to a well-established and consolidated field towards sustainable synthesis …
esoteric curiosity to a well-established and consolidated field towards sustainable synthesis …