Catalytic Asymmetric Mannich Reaction with N-Carbamoyl Imine Surrogates of Formaldehyde and Glyoxylate.

about

Catalytic Asymmetric Mannich Reaction with N-Carbamoyl Imine Surrogates of Formaldehyde and Glyoxylate.

Item

http://www.wikidata.org/entity/Q47695760

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Catalytic Asymmetric Mannich R ...... f Formaldehyde and Glyoxylate.

@en

Catalytic Asymmetric Mannich R ...... f Formaldehyde and Glyoxylate.

@nl

type

Item

label

Catalytic Asymmetric Mannich R ...... f Formaldehyde and Glyoxylate.

@en

Catalytic Asymmetric Mannich R ...... f Formaldehyde and Glyoxylate.

@nl

prefLabel

Catalytic Asymmetric Mannich R ...... f Formaldehyde and Glyoxylate.

@en

Catalytic Asymmetric Mannich R ...... f Formaldehyde and Glyoxylate.

@nl

P1476

Catalytic Asymmetric Mannich R ...... of Formaldehyde and Glyoxylate

@en

P2093

Linfeng Cui

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

Long Zhang

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

Xueling Mi

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

Yang'en You

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

P2860

Asymmetric Mannich synthesis of α-amino esters by anion-binding catalysis.

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

The direct catalytic asymmetric mannich reaction.

Direct Catalytic Asymmetric Mannich Reactions for the Construction of Quaternary Carbon Stereocenters.

Catalytic asymmetric direct Mannich reaction: a powerful tool for the synthesis of alpha,beta-diamino acids.

Reagent-controlled enantioselectivity switch for the asymmetric fluorination of β-ketocarbonyls by chiral primary amine catalysis.

A new approach to the asymmetric Mannich reaction catalyzed by chiral N,N'-dioxide-metal complexes.

Catalytic enantioselective formation of C-C bonds by addition to imines and hydrazones: a ten-year update.

α-Imino Esters in Organic Synthesis: Recent Advances.

Synthesis of vicinal aminoalcohols by stereoselective aza-Wacker cyclizations: access to (-)-acosamine by redox relay.

P304

13814-13818

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

P31

scholarly article

P356

10.1002/ANIE.201707005

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

Sanzhong Luo

P577

2017-10-02T00:00:00Z

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

P698

28887903

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