Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

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Application of Q2MM to predictions in stereoselective synthesis

P2860

Q57174851-D3D40102-D21D-4060-8671-5C7D98E8588B

P2860

Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

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http://www.wikidata.org/entity/Q51218319

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2016 nî lūn-bûn

@nan

2016年の論文

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2016年学术文章

@wuu

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh

2016年學術文章

@zh-hant

name

Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

@en

Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

@nl

type

Item

label

Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

@en

Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

@nl

prefLabel

Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

@en

Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

@nl

P1476

Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

@en

P2093

Liping Xu

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

Matthew S McCammant

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

Matthew S Sigman

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

Olaf Wiest

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

Xin Zhang

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

Yun-Dong Wu

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

P2860

Kinetic data for the transmetalation/reductive elimination in palladium-catalyzed Suzuki-Miyaura reactions: unexpected triple role of hydroxide ions used as base.

Palladium-catalyzed hydroarylation of 1,3-dienes with boronic esters via reductive formation of pi-allyl palladium intermediates under oxidative conditions.

A palladium-catalyzed three-component-coupling strategy for the differential vicinal diarylation of terminal 1,3-dienes.

Investigating the nature of palladium chain-walking in the enantioselective redox-relay Heck reaction of alkenyl alcohols

A palladium-catalyzed three-component cross-coupling of conjugated dienes or terminal alkenes with vinyl triflates and boronic acids

Universal solvation model based on solute electron density and on a continuum model of the solvent defined by the bulk dielectric constant and atomic surface tensions.

Synthesis of highly functionalized tri- and tetrasubstituted alkenes via Pd-catalyzed 1,2-hydrovinylation of terminal 1,3-dienes.

Development and Investigation of a Site Selective Palladium-Catalyzed 1,4-Difunctionalization of Isoprene using Pyridine-Oxazoline Ligands.

Imparting catalyst control upon classical palladium-catalyzed alkenyl C-H bond functionalization reactions

Palladium-catalyzed 1,4-difunctionalization of butadiene to form skipped polyenes

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scholarly article

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10.1021/ACS.JOC.6B01317

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

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English

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2016-08-03T00:00:00Z

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

P698

27486829

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

P921

isoprene

P932

5316510

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Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

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P2860

P2860

Mechanism and Selectivity in the Pd-Catalyzed Difunctionalization of Isoprene.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P31

P356

P407

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P407

P577

P698

P921

P932