Highly enantioselective Michael addition promoted by a new diterpene-derived bifunctional thiourea catalyst: a doubly stereocontrolled approach to chiral succinimide derivatives.

about

Diastereoselective addition of monoorganocuprates to a chiral fumarate: reaction development and synthesis of (-)-dihydroprotolichesterinic acid.Synthesis, cytotoxic activity, and 2D- and 3D-QSAR studies of 19-carboxyl-modified novel isosteviol derivatives as potential anticancer agents.

P2860

Q35926614-8B614AFE-ED16-4547-82E2-D230A4FE0E54 Q51094292-BC0BEC9F-8F7D-4706-8D0F-AD840D44348A

P2860

Highly enantioselective Michael addition promoted by a new diterpene-derived bifunctional thiourea catalyst: a doubly stereocontrolled approach to chiral succinimide derivatives.

Item

http://www.wikidata.org/entity/Q53639577

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年学术文章

@wuu

2014年学术文章

@zh-cn

2014年学术文章

@zh-hans

2014年学术文章

@zh-my

2014年学术文章

@zh-sg

2014年學術文章

@yue

2014年學術文章

@zh

2014年學術文章

@zh-hant

name

Highly enantioselective Michae ...... hiral succinimide derivatives.

@en

Highly enantioselective Michae ...... hiral succinimide derivatives.

@nl

type

Item

label

Highly enantioselective Michae ...... hiral succinimide derivatives.

@en

Highly enantioselective Michae ...... hiral succinimide derivatives.

@nl

prefLabel

Highly enantioselective Michae ...... hiral succinimide derivatives.

@en

Highly enantioselective Michae ...... hiral succinimide derivatives.

@nl

P1476

Highly enantioselective Michae ...... hiral succinimide derivatives.

@en

P2093

Chang-Hua Zhang

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

Hai-Long Du

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

Jing-Chao Tao

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

Tao Zhang

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

Zhi-Wei Ma

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

Zhong-Tai Song

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

P2860

A planning strategy for diversity-oriented synthesis

Discovering the mechanism of action of novel antibacterial agents through transcriptional profiling of conditional mutants.

Asymmetric catalysis by chiral hydrogen-bond donors.

Small-molecule H-bond donors in asymmetric catalysis.

Toggling enantioselective catalysis--a promising paradigm in the development of more efficient and versatile enantioselective synthetic methodologies.

Chiral multifunctional thiourea-phosphine catalyzed asymmetric [3 + 2] annulation of Morita-Baylis-Hillman carbonates with maleimides.

Chiral amines as organocatalysts for asymmetric conjugate addition to nitroolefins and vinyl sulfones via enamine activation.

(Thio)urea organocatalysis--what can be learnt from anion recognition?

Asymmetric organocatalytic addition reactions of maleimides: a promising approach towards the synthesis of chiral succinimide derivatives.

Cytotoxic labdane alkaloids from an ascidian Lissoclinum sp.: isolation, structure elucidation, and structure-activity relationship.

P304

121-127

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

P31

scholarly article

P356

10.1002/CHIR.22279

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

P433

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

P478

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

P577

2014-01-14T00:00:00Z

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

P698

24420919

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

P921

enantioselectivity

Highly enantioselective Michael addition promoted by a new diterpene-derived bifunctional thiourea catalyst: a doubly stereocontrolled approach to chiral succinimide derivatives.

about

P2860

P2860

Highly enantioselective Michael addition promoted by a new diterpene-derived bifunctional thiourea catalyst: a doubly stereocontrolled approach to chiral succinimide derivatives.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921