Enantioselective synthesis of novel pyrano[3,2-c]chromene derivatives as AChE inhibitors via an organocatalytic domino reaction.

about

Enantioselective synthesis of novel pyrano[3,2-c]chromene derivatives as AChE inhibitors via an organocatalytic domino reaction.

Item

http://www.wikidata.org/entity/Q47229588

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

Enantioselective synthesis of ...... ganocatalytic domino reaction.

@en

Enantioselective synthesis of ...... ganocatalytic domino reaction.

@nl

type

Item

label

Enantioselective synthesis of ...... ganocatalytic domino reaction.

@en

Enantioselective synthesis of ...... ganocatalytic domino reaction.

@nl

prefLabel

Enantioselective synthesis of ...... ganocatalytic domino reaction.

@en

Enantioselective synthesis of ...... ganocatalytic domino reaction.

@nl

P1476

Enantioselective synthesis of ...... ganocatalytic domino reaction.

@en

P2093

Baohua Xie

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

Chune Dong

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

Jie Zheng

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

Lu Yang

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

Ming He

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

Zhiye Hu

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

P2860

A new and rapid colorimetric determination of acetylcholinesterase activity

The crystal structure of a complex of acetylcholinesterase with a bis-(-)-nor-meptazinol derivative reveals disruption of the catalytic triad

AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility

Acetylcholinesterase inhibitors in Alzheimer's disease.

A Ligand-Based Drug Design. Discovery of 4-Trifluoromethyl-7,8-pyranocoumarin as a Selective Inhibitor of Human Cytochrome P450 1A2

Chiral squaramide derivatives are excellent hydrogen bond donor catalysts.

Development of cascade reactions for the concise construction of diverse heterocyclic architectures.

Applications of Chiral Squaramides: From Asymmetric Organocatalysis to Biologically Active Compounds.

Inhibiting β-amyloid-associated Alzheimer's pathogenesis in vitro and in vivo by a multifunctional dimeric bis(12)-hupyridone derived from its natural analogue.

Structure-activity relationship and molecular mechanisms of ethyl 2-amino-4-(2-ethoxy-2-oxoethyl)-6-phenyl-4h-chromene-3-carboxylate (sha 14-1) and its analogues.

P304

472-479

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

P31

scholarly article

P356

10.1039/C7OB02794J

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

P433

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

P478

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

P50

Hai-Bing Zhou

P577

2017-12-21T00:00:00Z

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

P698

29265146

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

P921

enantioselectivity