Phosphoramidites: privileged ligands in asymmetric catalysis
JF Teichert, BL Feringa - Angewandte Chemie International …, 2010 - Wiley Online Library
Asymmetric catalysis with transition‐metal complexes is the basis for a vast array of
stereoselective transformations and has changed the face of modern synthetic chemistry …
stereoselective transformations and has changed the face of modern synthetic chemistry …
Enantioselective copper-catalyzed conjugate addition and allylic substitution reactions
A Alexakis, JE Backvall, N Krause, O Pàmies… - Chemical …, 2008 - ACS Publications
In the past decades there has been a dramatic increase in the demand for enantiopure
compounds for fine-chemicals (ie, agrochemicals and pharmaceuticals) and material …
compounds for fine-chemicals (ie, agrochemicals and pharmaceuticals) and material …
[图书][B] Applied homogeneous catalysis with organometallic compounds: a comprehensive handbook in four volumes
B Cornils, WA Herrmann, M Beller, R Paciello - 2017 - books.google.com
The completely revised third edition of this four-volume classic is fully updated and now
includes such topics as as CH-activation and multicomponent reactions. It describes the …
includes such topics as as CH-activation and multicomponent reactions. It describes the …
Enantioselective conjugate additions
Enantioselective bond construction is a rapidly growing endeavor in the synthetic
community. This is in response to the increasing demand for enantiomerically pure …
community. This is in response to the increasing demand for enantiomerically pure …
Phosphoramidites: marvellous ligands in catalytic asymmetric conjugate addition
BL Feringa - Accounts of Chemical Research, 2000 - ACS Publications
The development of an efficient catalytic system for enantioselective carbon− carbon bond
formation by 1, 4-addition of organometallic reagents (organolithium, Grignard, and …
formation by 1, 4-addition of organometallic reagents (organolithium, Grignard, and …
Recent advances in catalytic enantioselective Michael additions
N Krause, A Hoffmann-Röder - Synthesis, 2001 - thieme-connect.com
This review summarizes the tremendous achievements in the field of catalytic
enantioselective Michael additions over the last few years. An impressive number of efficient …
enantioselective Michael additions over the last few years. An impressive number of efficient …
Asymmetric Michael additions to nitroalkenes
OM Berner, L Tedeschi, D Enders - European Journal of …, 2002 - Wiley Online Library
The asymmetric conjugate addition of various carbon and heteroatom nucleophiles to
nitroalkenes as a tool for the construction of highly functionalized synthetic building blocks is …
nitroalkenes as a tool for the construction of highly functionalized synthetic building blocks is …
Enantioselective organocatalytic Michael addition of malonate esters to nitro olefins using bifunctional cinchonine derivatives
J Ye, DJ Dixon, PS Hynes - Chemical communications, 2005 - pubs.rsc.org
A family of 9-amino (9-deoxy) epicinchonine derivatives, possessing a range of mono-and
bidentate hydrogen bond donor groups at the 9-position, were synthesised and evaluated …
bidentate hydrogen bond donor groups at the 9-position, were synthesised and evaluated …
Enantioselective copper‐catalysed conjugate addition
A Alexakis, C Benhaim - European Journal of Organic …, 2002 - Wiley Online Library
Enantioselective Copper‐Catalysed Conjugate Addition - Alexakis - 2002 - European Journal of
Organic Chemistry - Wiley Online Library Skip to Article Content Skip to Article Information …
Organic Chemistry - Wiley Online Library Skip to Article Content Skip to Article Information …
Catalytic asymmetric allylic and homoallylic diamination of terminal olefins via formal C− H activation
H Du, B Zhao, Y Shi - Journal of the American Chemical Society, 2008 - ACS Publications
This paper describes a catalytic asymmetric diamination process for terminal olefins at allylic
and homoallylic carbons via formal C− H activation using di-tert-butyldiaziridinone as …
and homoallylic carbons via formal C− H activation using di-tert-butyldiaziridinone as …