Enantiomerically Enriched (4+3) Cycloadducts from Optically Active Epoxy Enolsilanes

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Concerted Ring Opening and Cycloaddition of Chiral Epoxy Enolsilanes with Dienes Epoxy and aziridinyl enolsilanes in diastereoselective inter- and intramolecular Friedel–Crafts alkylations Asymmetric (4+3) Cycloadditions of Enantiomerically Enriched Epoxy Enolsilanes

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Enantiomerically Enriched (4+3) Cycloadducts from Optically Active Epoxy Enolsilanes

Item

http://www.wikidata.org/entity/Q59310151

description

wetenschappelijk artikel

@nl

наукова стаття, опублікована в липні 2012

@uk

name

Enantiomerically Enriched (4+3) Cycloadducts from Optically Active Epoxy Enolsilanes

@en

Enantiomerically Enriched

@nl

type

Item

label

Enantiomerically Enriched (4+3) Cycloadducts from Optically Active Epoxy Enolsilanes

@en

Enantiomerically Enriched

@nl

prefLabel

Enantiomerically Enriched (4+3) Cycloadducts from Optically Active Epoxy Enolsilanes

@en

Enantiomerically Enriched

@nl

P1476

Enantiomerically Enriched (4+3) Cycloadducts from Optically Active Epoxy Enolsilanes

@en

P2093

Brian Lo

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

Pauline Chiu

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

Sarah Lam

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

Wing-Tak Wong

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

P2860

Exploration of fundamental and synthetic aspects of the intramolecular 4 + 3 cycloaddition reaction.

Catalytic enantioselective peroxidation of alpha,beta-unsaturated ketones

(4+3) cycloaddition reactions of nitrogen-stabilized oxyallyl cations.

Asymmetric organocatalysis of 4 + 3 cycloaddition reactions.

Chiral Lewis acid-catalyzed highly enantioselective [4 + 3] cycloaddition reactions of nitrogen-stabilized oxyallyl cations derived from allenamides.

Inter- and intramolecular [4 + 3] cycloadditions using epoxy enol silanes as functionalized oxyallyl cation precursors.

Chiral allyl cations are captured by furan with 100% stereoselectivity: synthesis of enantiopure 2-alkoxy-8-oxabicyclo

P304

30-33

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

P31

scholarly article

P356

10.1002/AJOC.201200038

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

P433

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

P478

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

P577

2012-07-02T00:00:00Z

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

Enantiomerically Enriched (4+3) Cycloadducts from Optically Active Epoxy Enolsilanes

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P2860

P2860

Enantiomerically Enriched (4+3) Cycloadducts from Optically Active Epoxy Enolsilanes

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577