Approach to vicinal t-Boc-amino dibromides via catalytic aminobromination of nitrostyrenes without using chromatography and recrystallization.

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Catalytic Aminohalogenation of Alkenes and Alkynes.N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology.

P2860

Q36969250-FB8FA68D-05D1-4660-986F-A866B0E6B0F4 Q38293533-27653473-D488-4126-9AFA-D670046AF480

P2860

Approach to vicinal t-Boc-amino dibromides via catalytic aminobromination of nitrostyrenes without using chromatography and recrystallization.

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http://www.wikidata.org/entity/Q36600200

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

@zh-cn

name

Approach to vicinal t-Boc-amin ...... ography and recrystallization.

@ast

Approach to vicinal t-Boc-amin ...... ography and recrystallization.

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type

Item

label

Approach to vicinal t-Boc-amin ...... ography and recrystallization.

@ast

Approach to vicinal t-Boc-amin ...... ography and recrystallization.

@en

prefLabel

Approach to vicinal t-Boc-amin ...... ography and recrystallization.

@ast

Approach to vicinal t-Boc-amin ...... ography and recrystallization.

@en

P1476

Approach to vicinal t-Boc-amin ...... ography and recrystallization.

@en

P2093

Guigen Li

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

Hao Sun

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

Jianlin Han

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

Padmanabha V Kattamuri

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

Yi Pan

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 synthesis of α-amino-1,3-dithianes via chiral N-phosphonyl imine-based Umpolung reaction without using chromatography and recrystallization.

Catalytic enantioselective alkene aminohalogenation/cyclization involving atom transfer.

Asymmetric catalytic N-phosphonyl imine chemistry: the use of primary free amino acids and Et2AlCN for asymmetric catalytic Strecker reaction.

K3PO4-catalyzed regiospecific aminobromination of beta-nitrostyrene derivatives with N-bromoacetamide as aminobrominating agent.

Copper powder-catalyzed regio- and stereoselective aminobromination of alpha,beta-unsaturated ketones with TsNH2 and NBS as nitrogen and halogen sources.

Aminochlorination in water: first Brønsted acid-promoted synthesis of vicinal chloramines.

Asymmetric iodoamination of chalcones and 4-aryl-4-oxobutenoates catalyzed by a complex based on scandium(III) and a N,N'-dioxide ligand.

Catalytic asymmetric chloroamination reaction of α,β-unsaturated γ-keto esters and chalcones.

Unprecedented CO2-promoted aminochlorination of olefins with Chloramine-T.

P304

1171-1175

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P31

scholarly article

P356

10.1021/JO302727V

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English

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

P478

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

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2013-01-23T00:00:00Z

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P698

23311641

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P932

3568972

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

Approach to vicinal t-Boc-amino dibromides via catalytic aminobromination of nitrostyrenes without using chromatography and recrystallization.

about

P2860

P2860

Approach to vicinal t-Boc-amino dibromides via catalytic aminobromination of nitrostyrenes without using chromatography and recrystallization.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932