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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] [Diss]

Asymmetric Organocatalysis
script - [USA > e]

Asymmetric Organocatalysis
Slides - [USA > e]

Asymmetric Organocatalysis
Text - [USA > e]

Asymmetric Organocatalysis
Lecture notes - [USA > e]

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

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 - [CH > e]

Green Synthesis - 1
Principles of Green Chemistry/Synthesis; Catalytic Methods - Format: PDF - [USA > e]

Green Synthesis - 2
Catalytic Methods - Format: PDF - [USA > e]

Green Synthesis - 3
Unusual Forms of Energy in Synthesis - Format: PDF - [USA > e]

Grubbs’ Catalysts
Information. Sigma Aldrich - [e]

MacMillan's OrganoCatalysts™
Information. Sigma Aldrich - [e]

Metal-free catalysis by chiral Lewis bases
Article - [UK > e]

Noncovalent Organocatalysis
Article - Format: PDF - [CZ > e]

Organocatalysis
Almost Everything You Wanted to Know, but Never Asked ... - Format: PDF - [USA > e]

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

Organocatalysts for Asymmetric Reactions
Article - Format: PDF - [CN > e]

What is Organocatalysis?
Article - Format: PDF - [CA > e]

[Gen] [Diss]

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

Bifunctional Organocatalysts for Enantioselective aza-Morita-Baylis-Hillman Reaction
Article. Organic Chemistry Portal - [CH > e]

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

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

Iminium and enamine activation: methods for enantioselective organocatalysis
Dissertation 2005. Caltech - [USA > e]

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

Synthesis of Substituted Imidazoles via Organocatalysis
Article - [USA > e]

Total syntheses of the spiculisporic acids ...
Application of iminium activation technologies to natural product synthesis. Dissertation 2006. Caltech - [USA > e]