The Allylic Trihaloacetimidate Rearrangement - sprookjes - yvandenbroek - TriplyDB

The Allylic Trihaloacetimidate Rearrangement

The Allylic Trihaloacetimidate Rearrangement

http://www.wikidata.org/entity/Q56068600

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Enantioselective Total Synthesis of (+)-Neostenine.A highly enantioselective Overman rearrangement through asymmetric counteranion-directed palladium catalysis.Synthesis of Chiral, Enantiopure Allylic Amines by the Julia Olefination of α-Amino Esters

P2860

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The Allylic Trihaloacetimidate Rearrangement

http://www.wikidata.org/entity/Q56068600

description

wetenschappelijk artikel

@nl

наукова стаття, опублікована в серпні 2005

@uk

name

The Allylic Trihaloacetimidate Rearrangement

@en

The Allylic Trihaloacetimidate Rearrangement

@nl

type

label

The Allylic Trihaloacetimidate Rearrangement

@en

The Allylic Trihaloacetimidate Rearrangement

@nl

prefLabel

The Allylic Trihaloacetimidate Rearrangement

@en

The Allylic Trihaloacetimidate Rearrangement

@nl

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0471264180.OR066.01

P1476

The Allylic Trihaloacetimidate Rearrangement

@en

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Larry E. Overman

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

Nancy E. Carpenter

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

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Metal-Initiated Amination of Alkenes and Alkynes

A general, highly enantioselective method for the synthesis of D and L alpha-amino acids and allylic amines

Directed dihydroxylation of cyclic allylic alcohols and trichloroacetamides using OsO4/TMEDA

Allylic 1,3-strain as a controlling factor in stereoselective transformations

Catalytic Asymmetric Rearrangement of Allylic Trichloroacetimidates. A Practical Method for Preparing Allylic Amines and Congeners of High Enantiomeric Purity

Synthesis of new cyclitol compounds that influence the activity of phosphatidylinositol 4-kinase isoform, PI4K230.

Improved Conditions for Facile Overman Rearrangement(1).

Highly regio- and enantioselective palladium-catalyzed allylic amination with sodium diformylamide.

Iridium complex-catalyzed allylic amination of allylic esters.

Synthesis of 2,3-disubstituted pyrroles from 3,N-dilithio-N-(tert-butyldimethylsilyl)-2-buten-1-amine.

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1-107

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

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scholarly article

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10.1002/0471264180.OR066.01

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

P577

2005-08-26T00:00:00Z

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

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228033887

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