Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction.

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Passerini Reactions on Biocatalytically Derived Chiral Azetidines.Multicomponent, fragment-based synthesis of polyphenol-containing peptidomimetics and their inhibiting activity on beta-amyloid oligomerization.

P2860

Q30313891-0316C5D3-E7ED-443E-A475-97F275D574BE Q47583431-7115F66B-4356-4CEA-9117-0DA0201F504A

P2860

Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction.

Item

http://www.wikidata.org/entity/Q42539117

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Diastereoselective Ugi reactio ...... anocatalytic Mannich reaction.

@en

Diastereoselective Ugi reactio ...... anocatalytic Mannich reaction.

@nl

type

Item

label

Diastereoselective Ugi reactio ...... anocatalytic Mannich reaction.

@en

Diastereoselective Ugi reactio ...... anocatalytic Mannich reaction.

@nl

prefLabel

Diastereoselective Ugi reactio ...... anocatalytic Mannich reaction.

@en

Diastereoselective Ugi reactio ...... anocatalytic Mannich reaction.

@nl

P1476

Diastereoselective Ugi reactio ...... ganocatalytic Mannich reaction

@en

P2093

Samantha Caputo

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

Valeria Rocca

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

P2860

Three-component asymmetric catalytic Ugi reaction--concinnity from diversity by substrate-mediated catalyst assembly.

Recent developments in asymmetric multicomponent reactions.

Metal-mediated post-Ugi transformations for the construction of diverse heterocyclic scaffolds.

Multicomponent reactions in fungicide research: the discovery of mandipropamid.

An asymmetric Ugi three-component reaction induced by chiral cyclic imines: synthesis of morpholin- or piperazine-keto-carboxamide derivatives.

Enantio- and diastereoselective synthesis of highly substituted benzazepines by a multicomponent strategy coupled with organocatalytic and enzymatic procedures.

The homo-PADAM protocol: stereoselective and operationally simple synthesis of α-oxo- or α-hydroxy-γ-acylaminoamides and chromanes.

P304

139-143

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P31

scholarly article

P356

10.3762/BJOC.12.15

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P478

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

P50

P577

2016-01-26T00:00:00Z

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P5875

292073015

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P698

26877816

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P921

diastereoselectivity

P932

4734417

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Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction.

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P2860

P2860

Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P5875

P698

P921

P932