Cinchonidinium acetate as a convenient catalyst for the asymmetric synthesis of cis-stilbenediamines.

about

Computational insight into the cooperative role of non-covalent interactions in the aza-Henry reaction catalyzed by quinine derivatives: mechanism and enantioselectivity.One-pot multicomponent nitro-Mannich reaction using a heterogeneous catalyst under solvent-free conditions.

P2860

Q48673593-FF49FE31-278D-453A-A2F6-9E21119B4802 Q55393704-4F10C48F-6135-499A-ACEC-632FD32307B2

P2860

Cinchonidinium acetate as a convenient catalyst for the asymmetric synthesis of cis-stilbenediamines.

Item

http://www.wikidata.org/entity/Q35668427

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Cinchonidinium acetate as a co ...... hesis of cis-stilbenediamines.

@ast

Cinchonidinium acetate as a co ...... hesis of cis-stilbenediamines.

@en

type

Item

label

Cinchonidinium acetate as a co ...... hesis of cis-stilbenediamines.

@ast

Cinchonidinium acetate as a co ...... hesis of cis-stilbenediamines.

@en

prefLabel

Cinchonidinium acetate as a co ...... hesis of cis-stilbenediamines.

@ast

Cinchonidinium acetate as a co ...... hesis of cis-stilbenediamines.

@en

P1476

Cinchonidinium acetate as a co ...... hesis of cis-stilbenediamines.

@en

P2093

Marisa C Kozlowski

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

Ryan R Walvoord

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

P2860

Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry

Organocatalytic, diastereo- and enantioselective synthesis of nonsymmetric cis-stilbene diamines: a platform for the preparation of single-enantiomer cis-imidazolines for protein-protein inhibition.

Enantioselective Michael reaction of malonates to nitroolefins catalyzed by bifunctional organocatalysts.

Medicinal agents incorporating the 1,2-diamine functionality.

Alpha,beta-diamino acids: biological significance and synthetic approaches.

Preparation of (-)-Nutlin-3 using enantioselective organocatalysis at decagram scale.

Nitro-Mannich reaction.

Catalytic, Enantioselective Synthesis of Stilbene cis-Diamines: A Concise Preparation of (-)-Nutlin-3, a Potent p53/MDM2 Inhibitor.

Catalysis of the Michael addition reaction by late transition metal complexes of BINOL-derived salens.

Asymmetric aza-Henry reaction under phase transfer catalysis: an experimental and theoretical study.

P304

3070-3074

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

P31

scholarly article

P356

10.1016/J.TETLET.2014.12.105

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

P433

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

P478

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

P577

2015-06-01T00:00:00Z

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

P698

26041941

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

P932

4450089

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

Cinchonidinium acetate as a convenient catalyst for the asymmetric synthesis of cis-stilbenediamines.

about

P2860

P2860

Cinchonidinium acetate as a convenient catalyst for the asymmetric synthesis of cis-stilbenediamines.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932