(Q56988565)

English

Controlling stereoselectivity in the aminocatalytic enantioselective Mannich reaction of aldehydes with in situ generated N-carbamoyl imines

scientific article published on 01 May 2010

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Controlling stereoselectivity in the aminocatalytic enantioselective Mannich reaction of aldehydes with in situ generated N-carbamoyl imines (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

enantioselectivity

1 reference

based on heuristic

inferred from title

stereoselectivity

1 reference

based on heuristic

inferred from title

Giorgio Bencivenni

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Paolo Melchiorre

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Patrizia Galzerano

1

object named as

Patrizia Galzerano

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

4

object named as

Letizia Sambri

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

author name string

Dario Agostino

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Giuseppe Bartoli

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

language of work or name

0 references

publication date

1 May 2010

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Chemistry—A European Journal

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

16

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

6069-6076

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

20

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Emil Knoevenagel und die Ursprünge der Aminokatalyse

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Emil Knoevenagel and the roots of aminocatalysis

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Asymmetric aminocatalysis--gold rush in organic chemistry

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Organocatalysis lost: modern chemistry, ancient chemistry, and an unseen biosynthetic apparatus.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Asymmetric enamine catalysis

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Light in aminocatalysis: the asymmetric intermolecular alpha-alkylation of aldehydes

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

The advent and development of organocatalysis

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Catalytic enantioselective cross-Mannich reaction of aldehydes.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Organocatalysed asymmetric Mannich reactions

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

The direct and enantioselective, one-pot, three-component, cross-mannich reaction of aldehydes.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

The direct organocatalytic asymmetric mannich reaction: unmodified aldehydes as nucleophiles

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

The Direct catalytic asymmetric cross-Mannich reaction: a highly enantioselective route to 3-amino alcohols and alpha-amino acid derivatives

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

A solid-supported organocatalyst for highly stereoselective, batch, and continuous-flow Mannich reactions.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

A general organocatalyst for direct alpha-functionalization of aldehydes: stereoselective C-C, C-N, C-F, C-Br, and C-S bond-forming reactions. Scope and mechanistic insights

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

anti-selective direct asymmetric Mannich reactions catalyzed by axially chiral amino sulfonamide as an organocatalyst

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Direct asymmetric anti-Mannich-type reactions catalyzed by a designed amino acid

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Catalysis of 3-pyrrolidinecarboxylic acid and related pyrrolidine derivatives in enantioselective anti-Mannich-type reactions: importance of the 3-acid group on pyrrolidine for stereocontrol

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Proline-catalyzed highly enantioselective and anti-selective Mannich reaction of unactivated ketones: synthesis of chiral alpha-amino acids

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Proline-catalyzed asymmetric formal alpha-alkylation of aldehydes via vinylogous iminium ion intermediates generated from arylsulfonyl indoles

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Asymmetric iminium ion catalysis with a novel bifunctional primary amine thiourea: controlling adjacent quaternary and tertiary stereocenters

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Targeting structural and stereochemical complexity by organocascade catalysis: construction of spirocyclic oxindoles having multiple stereocenters

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Asymmetric organocatalytic cascade reactions with alpha-substituted alpha,beta-unsaturated aldehydes

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Phase-transfer-catalyzed asymmetric aza-Henry reaction using N-carbamoyl imines generated in situ from alpha-amido sulfones

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Catalytic enantioselective aza-Henry reaction with broad substrate scope.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Aminocatalytic enantioselective anti-Mannich reaction of aldehydes with in situ generated N-Cbz and N-Boc imines

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

A designer axially chiral amino sulfonamide as an efficient organocatalyst for direct asymmetric mannich reactions of N-Boc-protected imines

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

A designer axially chiral amino sulfonamide as an efficient organocatalyst for direct asymmetric anti-selective Mannich reactions and syn-selective cross-aldol reactions.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Organocatalysis with proline derivatives: improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Expedient Synthesis of Chiral 1,2- and 1,4-Diamines: Protecting Group Dependent Regioselectivity in Direct Organocatalytic Asymmetric Mannich Reactions

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Diphenylprolinol silyl ethers as efficient organocatalysts for the asymmetric Michael reaction of aldehydes and nitroalkenes.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Alpha,alpha-diarylprolinol ethers: new tools for functionalization of carbonyl compounds.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Direct organocatalytic and highly enantio- and diastereoselective Mannich reactions of alpha-substituted alpha-cyanoacetates

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Proline-catalysed Mannich reactions of acetaldehyde.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Direct organocatalytic mannich reaction of acetaldehyde: an improved catalyst and mechanistic insight from a computational study

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

The proline-catalyzed double Mannich reaction of acetaldehyde with N-Boc imines

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Organocatalytic reactions with acetaldehyde

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Towards the optimal screening collection: a synthesis strategy

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Proline-catalyzed asymmetric reactions

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Chemistry. The simplest "enzyme".

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.200903217

21 January 2018

Identifiers

10.1002/CHEM.200903217

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20397160%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q56988565&oldid=1835173005"