Chiral aminophosphines as catalysts for enantioselective double-Michael indoline syntheses

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Chiral phosphines in nucleophilic organocatalysis Synthesis of a Library of 1,5,2-Dithiazepine 1,1-Dioxides. Part 1: A One-Pot Sulfonylation/Thia-Michael Protocol.Nucleophilic Chiral Phosphines: Powerful and Versatile Catalysts for Asymmetric Annulations

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Chiral aminophosphines as catalysts for enantioselective double-Michael indoline syntheses

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http://www.wikidata.org/entity/Q41823492

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2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

name

Chiral aminophosphines as cata ...... ble-Michael indoline syntheses

@en

type

Item

label

Chiral aminophosphines as cata ...... ble-Michael indoline syntheses

@en

prefLabel

Chiral aminophosphines as cata ...... ble-Michael indoline syntheses

@en

P1476

Chiral aminophosphines as cata ...... ble-Michael indoline syntheses

@en

P2093

Ohyun Kwon

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

San N Khong

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

P2860

3,4-Dihydropyrimido(1,2-a)indol-10(2H)-ones as potent non-peptidic inhibitors of caspase-3

The advent and development of organocatalysis

Diversity-oriented synthesis based on the DPPP-catalyzed mixed double-Michael reactions of electron-deficient acetylenes and β-amino alcohols.

Modified BINOL ligands in asymmetric catalysis.

Diphosphine-catalyzed mixed double-Michael reaction: a unified synthesis of indolines, dihydropyrrolopyridines, benzimidazolines, tetrahydroquinolines, tetrahydroisoquinolines, dihydrobenzo-1,4-oxazines, and dihydrobenzo-3,1-oxazines

Bisphosphine-catalyzed mixed double-Michael reactions: asymmetric synthesis of oxazolidines, thiazolidines, and pyrrolidines.

4-Phenylbutanoyl-2(S)-acylpyrrolidines and 4-phenylbutanoyl-L-prolyl-2(S)-acylpyrrolidines as prolyl oligopeptidase inhibitors.

P(RNCH(2)CH(2))(3)N: efficient 1,4-addition catalysts.

An efficient procedure for the preparation of (E)-alpha-alkylidenecycloalkanones mediated by a CeCl(3) x 7H(2)O-NaI system. Novel methodology for the synthesis of (S)-(-)-pulegone.

Design of N-spiro C2-symmetric chiral quaternary ammonium bromides as novel chiral phase-transfer catalysts: synthesis and application to practical asymmetric synthesis of alpha-amino acids.

P304

5626-5650

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P31

scholarly article

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10.3390/MOLECULES17055626

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P407

English

P433

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

P478

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

P577

2012-05-11T00:00:00Z

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

P5875

224949651

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

P698

22580397

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

P921

enantioselectivity

P932

4091971

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

Chiral aminophosphines as catalysts for enantioselective double-Michael indoline syntheses

about

P2860

P2860

Chiral aminophosphines as catalysts for enantioselective double-Michael indoline syntheses

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P921

P932