Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

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N,N'-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea: a privileged motif for catalyst development.Hydrazones as Singular Reagents in Asymmetric Organocatalysis.

P2860

Q38202902-5AD0A07C-064B-4916-AD7F-80AEE8467181 Q38934959-E5C686DB-B120-489D-AB6F-886CC315C294

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Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

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http://www.wikidata.org/entity/Q46264788

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2013 nî lūn-bûn

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2013年の論文

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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

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2013年學術文章

@zh

2013年學術文章

@zh-hant

name

Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

@en

Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

@nl

type

Item

label

Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

@en

Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

@nl

prefLabel

Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

@en

Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

@nl

P1476

Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

@en

P2093

Aurora Martínez-Muñoz

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

David Monge

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

Eloísa Martín-Zamora

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

Eugenia Marqués-López

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

Asymmetric Strecker Reactions

Scaleable catalytic asymmetric Strecker syntheses of unnatural α-amino acids

Design and synthesis of a CD4 beta-turn mimetic that inhibits human immunodeficiency virus envelope glycoprotein gp120 binding and infection of human lymphocytes.

A General Catalyst for the Asymmetric Strecker Reaction This work was supported by the NIH (GM-43214). A postdoctoral fellowship to M.S.S. (NIH), and a predoctoral fellowship to P.V. sponsored by Alfred Bader are gratefully acknowledged.

N,N-dialkylhydrazones in organic synthesis. From simple N,N-dimethylhydrazones to supported chiral auxiliaries.

Metal-free, noncovalent catalysis of diels-alder reactions by neutral hydrogen bond donors in organic solvents and in water.

Asymmetric catalysis by chiral hydrogen-bond donors.

Organocatalysis mediated by (thio)urea derivatives.

Small-molecule H-bond donors in asymmetric catalysis.

P304

8247-8255

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P31

scholarly article

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10.1039/C3OB41437J

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

P433

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

P478

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

P50

Eleuterio Álvarez

Rosario Fernández

José M Lassaletta

P577

2013-10-28T00:00:00Z

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

P698

24165968

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Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

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P2860

P2860

Asymmetric organocatalytic Strecker-type reactions of aliphatic N,N-dialkylhydrazones.

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698