Organocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o-Formyl-β-nitrostyrenes.

about

Organocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o-Formyl-β-nitrostyrenes.

Item

http://www.wikidata.org/entity/Q41587304

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

Organocatalytic Asymmetric Dom ...... with o-Formyl-β-nitrostyrenes.

@en

type

Item

label

Organocatalytic Asymmetric Dom ...... with o-Formyl-β-nitrostyrenes.

@en

prefLabel

Organocatalytic Asymmetric Dom ...... with o-Formyl-β-nitrostyrenes.

@en

P1476

Organocatalytic Asymmetric Dom ...... with o-Formyl-β-nitrostyrenes.

@en

P2093

Dieter Enders

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

Gerhard Raabe

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

Pankaj Chauhan

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

Server Uzungelis

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

Suruchi Mahajan

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

P2860

Asymmetric Organocatalytic Domino Reactions

Notoamide O, a structurally unprecedented prenylated indole alkaloid, and notoamides P-R from a marine-derived fungus, Aspergillus sp.

Highly enantioselective conjugate addition of nitromethane to chalcones using bifunctional cinchona organocatalysts.

Organocatalysis: asymmetric cascade reactions catalysed by chiral secondary amines.

Chiral squaramide derivatives are excellent hydrogen bond donor catalysts.

Squaramide-catalyzed enantioselective Michael addition of diphenyl phosphite to nitroalkenes.

Enantioselective synthesis of substituted oxindoles and spirooxindoles with applications in drug discovery.

Organocatalytic cascade reactions as a new tool in total synthesis.

Squaramides: physical properties, synthesis and applications.

Asymmetric organocatalytic cyclization and cycloaddition reactions.

P304

1024-1031

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

P31

scholarly article

P356

10.1055/S-0034-1379943

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

P433

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

P478

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

P50

Charles C J Loh

P577

2015-04-01T00:00:00Z

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

P698

26722133

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

P932

4693955

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