Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

about

Dynamic kinetic resolution of 2,3-dihydrobenzo[b]furans: chemoenzymatic synthesis of analgesic agent BRL 37959

P2860

Q56927629-D80681C2-098C-4221-AB60-10DFBEA72736

P2860

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

Item

http://www.wikidata.org/entity/Q42792294

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

2010年论文

@zh

2010年论文

@zh-cn

name

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

@en

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

@nl

type

Item

label

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

@en

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

@nl

prefLabel

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

@en

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

@nl

P1476

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

@en

P2093

Robert Christian Simon

http://www.w3.org/2001/XMLSchema#string

P2860

Enantioselective organocatalysis

Are Oxazolidinones Really Unproductive, Parasitic Species in Proline Catalysis? – Thoughts and Experiments Pointing to an Alternative View

Asymmetric Catalysis Special Feature Part II: New mechanistic studies on the proline-catalyzed aldol reaction

Introduction: Organocatalysis

In the Golden Age of Organocatalysis

Kinetic and Stereochemical Evidence for the Involvement of Only One Proline Molecule in the Transition States of Proline-Catalyzed Intra- and Intermolecular Aldol Reactions

The proline-catalyzed direct asymmetric three-component Mannich reaction: scope, optimization, and application to the highly enantioselective synthesis of 1,2-amino alcohols.

A highly enantioselective route to either enantiomer of both alpha- and beta-amino acid derivatives.

Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-alder reactions.

Asymmetric organocatalysis.

P304

14534-14544

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/CHEM.201002130

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Jörg Pietruszka

P577

2010-12-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

21108254

http://www.w3.org/2001/XMLSchema#string

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

about

P2860

P2860

Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698