Results 281 to 290 of about 16,879 (311)
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Alkynes in Organocatalysis

Asian Journal of Organic Chemistry, 2014
AbstractIn this Focus Review, a selection of organocatalyzed reactions in which alkynes have been used are presented. Catalysis by tertiary and secondary amines, by phase‐transfer catalysis, by phosphines and carbenes, as well as bifunctional and multiple catalysis are discussed.
SALVIO, RICCARDO   +2 more
openaire   +5 more sources

Enantioselective Organocatalysis

Angewandte Chemie International Edition, 2001
The last few years have witnessed a spectacular advancement in new catalytic methods based on metal-free organic molecules. In many cases, these small compounds give rise to extremely high enantioselectivities. Preparative advantages are notable: usually the reactions can be performed under an aerobic atmosphere with wet solvents.
Peter I., Dalko, Lionel, Moisan
openaire   +2 more sources

Radicals in Asymmetric Organocatalysis

Angewandte Chemie International Edition, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Bertelsen, Søren   +2 more
openaire   +5 more sources

Enantioselective organocatalysis

Drug Discovery Today, 2007
Enantioselective organocatalysis has emerged as a powerful synthetic paradigm that is complementary to metal-catalysed transformations and has accelerated the development of new methods to make diverse chiral molecules. The operational simplicity, ready availability of catalysts and low toxicity associated with organocatalysis makes it an attractive ...
Matthew J, Gaunt   +3 more
openaire   +2 more sources

Organocatalysis in Inert C-H Bond Functionalization.

Chemical Reviews, 2017
As two coexisting and fast-growing research fields in modern synthetic chemistry, the merging of organocatalysis and C-H bond functionalization is well foreseeable, and the joint force along this line has been demonstrated to be a powerful approach in ...
Yan Qin, Lihui Zhu, S. Luo
semanticscholar   +1 more source

Organocatalysis by N-heterocyclic carbenes.

Chemical Reviews, 2007
In the investigation of efficient chemical transformations, the carbon-carbon bond-forming reactions play an outstanding role. In this context, organocatalytic processes have achieved considerable attention.
D. Enders, O. Niemeier, A. Henseler
semanticscholar   +1 more source

Enantioconvergent Substitution Reactions of Racemic Electrophiles by Organocatalysis.

Chemistry, 2021
Over the past decades, the development of enantioselective catalysis using organocatalysts has evolved into an active research field and a number of enantioselective transformations have been established.
J. Kikuchi, M. Terada
semanticscholar   +1 more source

ChemInform Abstract: New Concepts for Organocatalysis

ChemInform, 2008
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Benjamin List, Subhas Chandra Pan
openaire   +4 more sources

Aerobic Oxidative C-H Azolation of Indoles and One-Pot Synthesis of Azolyl Thioindoles by Flavin-Iodine-Coupled Organocatalysis.

Organic Letters, 2021
The aerobic oxidative cross-coupling of indoles with azoles driven by flavin-iodine-coupled organocatalysis has been developed for the green synthesis of 2-(azol-1-yl)indoles.
Kazumasa Tanimoto   +4 more
semanticscholar   +1 more source

Single Electron Transfer Reactions Enabled by N-Heterocyclic Carbene Organocatalysis.

Chemistry, 2020
Over the past decades, N -heterocyclic carbene (NHC) organocatalysis has undergone flourish development on the basis of closed-shell reaction paths. By contrast, the emerging area of single electron transfer (SET) reactions enabled by NHC catalysis still
Qing-Zhu Li   +3 more
semanticscholar   +1 more source

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