A method for the deprotection of alkylpinacolyl boronate esters. - Wikidata - wikimedia - TriplyDB

A method for the deprotection of alkylpinacolyl boronate esters.

A method for the deprotection of alkylpinacolyl boronate esters.

http://www.wikidata.org/entity/Q34974814

about

Towards Selective Mycobacterial ClpP1P2 Inhibitors with Reduced Activity against the Human Proteasome.Boryl (Hetero)aryne Precursors as Versatile Arylation Reagents: Synthesis through C-H Activation and Orthogonal Reactivity.Prochelator BHAPI protects cells against paraquat-induced damage by ROS-triggered iron chelation Selection of boron reagents for Suzuki-Miyaura coupling.A catalytic, enantioselective formal synthesis of (+)-dichroanone and (+)-taiwaniaquinone H.Iterative reactions of transient boronic acids enable sequential C-C bond formation.Alkylboronic esters from copper-catalyzed borylation of primary and secondary alkyl halides and pseudohalides.Copper-catalyzed synthesis of allenylboronic acids. Access to sterically encumbered homopropargylic alcohols and amines by propargylboration.

P2860

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P2860

A method for the deprotection of alkylpinacolyl boronate esters.

http://www.wikidata.org/entity/Q34974814

description

2011 nî lūn-bûn

@nan

2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年学术文章

@wuu

2011年学术文章

@zh-cn

2011年学术文章

@zh-hans

2011年学术文章

@zh-my

2011年学术文章

@zh-sg

2011年學術文章

@yue

name

A method for the deprotection of alkylpinacolyl boronate esters.

@ast

A method for the deprotection of alkylpinacolyl boronate esters.

@en

A method for the deprotection of alkylpinacolyl boronate esters.

@nl

type

label

A method for the deprotection of alkylpinacolyl boronate esters.

@ast

A method for the deprotection of alkylpinacolyl boronate esters.

@en

A method for the deprotection of alkylpinacolyl boronate esters.

@nl

prefLabel

A method for the deprotection of alkylpinacolyl boronate esters.

@ast

A method for the deprotection of alkylpinacolyl boronate esters.

@en

A method for the deprotection of alkylpinacolyl boronate esters.

@nl

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P1433

Journal of Organic Chemistry

P1476

A method for the deprotection of alkylpinacolyl boronate esters.

@en

P2093

Jing Sun

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

Michael T Perfetti

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P2860

Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands.

Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction.

Efficient hydrolysis of organotrifluoroborates via silica gel and water.

Structure-activity relationships of boronic acid inhibitors of dipeptidyl peptidase IV. 1. Variation of the P2 position of Xaa-boroPro dipeptides.

Palladium-catalyzed, direct boronic acid synthesis from aryl chlorides: a simplified route to diverse boronate ester derivatives.

Neopentylglycolborylation of ortho-substituted aryl halides catalyzed by NiCl(2)-based mixed-ligand systems.

N-Terminal peptidic boronic acids selectively inhibit human ClpXP.

A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.

Multistep synthesis of complex boronic acids from simple MIDA boronates.

The first example of enamine-Lewis acid cooperative bifunctional catalysis: application to the asymmetric aldol reaction.

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3571-3575

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scholarly article

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10.1021/JO200250Y

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9

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76

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Webster L Santos

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50935227

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3092631

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