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Organocatalysis



Organocatalysis

Organocatalysis is a organic chemistry term for a special form of catalysis in which a chemical reaction rate is increased by an organic compound (the organocatalyst).

Online available information on organocatalysis and organocatalytic reactions.

Further information categories about related topics are listed in the navigation menu on the left side of these page.



[Gen] [Lec] [Diss]

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General Information


Asymmetric Organocatalysis
… using chiral amines - Format: PDF

Asymmetric Organocatalysis
Seminar script

Asymmetric Organocatalysis
Slides

Asymmetric Organocatalysis
Text

Asymmetric Organocatalysis
… emphasis on enamine catalysis

Asymmetric Organocatalysis
Lecture notes - Format: PDF

Asymmetric Organocatalysis
eBooklet: Synthetic Methods. Sigma Aldrich - Format: PDF

Enantioselective organocatalysis
This article shows how enantioselective organocatalysis can represent a powerful, complementary paradigm to metal-catalysed enantiolselective synthesis in the preparation of single enantiomers of chiral drug molecules for screening and clinical trials

Grubbs’ Catalysts
Information. Sigma Aldrich

MacMillan's OrganoCatalysts™
Information. Sigma Aldrich

Metal-free catalysis by chiral Lewis bases
Article

Noncovalent Organocatalysis
Article - Format: PDF

Organocatalysis
Organocatalysis uses small organic molecules predominantly composed of C, H, O, N, S and P to accelerate chemical reactions. Organic Chemistry Portal

Organocatalysis
Almost Everything You Wanted to Know, but Never Asked ... - Format: PDF

Organocatalysts for Asymmetric Reactions
Article - Format: PDF

What is Organocatalysis?
Article - Format: PDF



[Gen] [Lec] [Diss]

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Lecture Notes, Tutorials


Asymmetric Organocatalysis
Emphasis on Enamine catalysis - Format: PDF

Chiral Organocatalysis
Lecture notes - Format: PDF

Trifunctional Organocatalysis
Article, 2009 - Format: PDF



[Gen] [Lec] [Diss]

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Dissertations


A Highly Enantioselective Lewis Basic Organocatalyst
... for Reduction of N-Aryl Imines with Unprecedented Substrate Spectrum. Organic Chemistry Portal

Bifunctional Organocatalysts for Enantioselective aza-Morita-Baylis-Hillman Reaction
Article. Organic Chemistry Portal

Chiral 2,2'-Bipyridine-Type N-Monoxides
... as Organocatalysts in the Enantioselective Allylation of Aldehydes with Allyltrichlorosilane. Organic Chemistry Portal

High Substrate/Catalyst Organocatalysis ...
... by a Chiral Brønsted Acid for an Enantioselective Aza-Ene-Type Reaction. Organic Chemistry Portal

Iminium and enamine activation: methods for enantioselective organocatalysis
Dissertation 2005. Caltech, USA

New Concepts for Enantioselective Organocatalysis and Transition-Metal Catalysis
Chiral-at-Rhenium Donor Ligands as Design Elements. Dissertation 2006. University of Erlangen

Synthesis of Substituted Imidazoles via Organocatalysis
Article

Theoretical Studies in Nucleophilic Organocatalysis
Dissertation, 2009. Munich University

Total syntheses of the spiculisporic acids ...
Application of iminium activation technologies to natural product synthesis. Dissertation 2006. Caltech, USA







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Citation:
www.internetchemistry.com/chemistry/organocatalysis.htm
Entries:
28
Topic:
Organocatalysis
Keywords:
Organocatalysis, Organocatalysts, organic, chemistry, reactions
Update:
25.02.2012 00:00:00 [link check]
 
25.02.2012 [site update]


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Related Books and Scientific Literature: Organocatalysis:


Buchempfehlung

Peter I. Dalko

Enantioselective Organocatalysis: Reactions and Experimental Procedures

In this reference leaders at the forefront of research provide an insight into one of the hottest topics in organic synthesis, focusing on the most important enantioselective reactions. Clearly structured, each entry begins with a concise introduction, including a mechanistic discussion of the reaction, followed by preparative guidelines for newcomers, such as carefully selected working procedures with critical notes for bench chemists, rules of thumb and tips and tricks.

Wiley-VCH; 2007


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