Enantio- and periselective nitroalkene Diels-Alder reactions catalyzed by helical-chiral hydrogen bond donor catalysts.

about

Enantio- and periselective nitroalkene Diels-Alder reactions catalyzed by helical-chiral hydrogen bond donor catalysts.

Item

http://www.wikidata.org/entity/Q44713026

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

@zh

2013年學術文章

@zh-hant

name

Enantio- and periselective nit ...... hydrogen bond donor catalysts.

@en

Enantio- and periselective nit ...... hydrogen bond donor catalysts.

@nl

type

Item

label

Enantio- and periselective nit ...... hydrogen bond donor catalysts.

@en

Enantio- and periselective nit ...... hydrogen bond donor catalysts.

@nl

prefLabel

Enantio- and periselective nit ...... hydrogen bond donor catalysts.

@en

Enantio- and periselective nit ...... hydrogen bond donor catalysts.

@nl

P1476

Enantio- and periselective nit ...... hydrogen bond donor catalysts

@en

P2093

Maurice J Narcis

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

Zhili Peng

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

P2860

Asymmetric Diels-Alder reactions catalyzed by a triflic acid activated chiral oxazaborolidine

Applications of helical-chiral pyridines as organocatalysts in asymmetric synthesis.

Enantioselective [3 + 2] cycloaddition of allenes to acrylates catalyzed by dipeptide-derived phosphines: facile creation of functionalized cyclopentenes containing quaternary stereogenic centers.

Asymmetric catalysis by chiral hydrogen-bond donors.

Small-molecule H-bond donors in asymmetric catalysis.

Application of a new chiral phosphepine to the catalytic asymmetric synthesis of highly functionalized cyclopentenes that bear an array of heteroatom-substituted quaternary stereocenters.

Catalytic Asymmetric [4 + 2] Additions with Aliphatic Nitroalkenes.

Iminium catalysis.

Hydrogen-bond-mediated asymmetric catalysis.

Cationic-oxazaborolidine-catalyzed enantioselective Diels-Alder reaction of alpha,beta-unsaturated acetylenic ketones.

P304

9982-9998

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

P31

scholarly article

P356

10.3390/MOLECULES18089982

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

Norito Takenaka

P577

2013-08-19T00:00:00Z

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

P5875

256076161

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

P698

23966083

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

P932

6270221

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