Cobalt-Catalyzed 1,1-Diboration of Terminal Alkynes: Scope, Mechanism, and Synthetic Applications.

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Cobalt-Catalyzed Diborylation of 1,1-disubstituted Vinylarenes: A Practical Route to Branched gem-Bis(boryl)alkanes.Cobalt-catalysed Markovnikov selective hydroboration of vinylarenes.

P2860

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P2860

Cobalt-Catalyzed 1,1-Diboration of Terminal Alkynes: Scope, Mechanism, and Synthetic Applications.

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http://www.wikidata.org/entity/Q48234511

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Cobalt-Catalyzed 1,1-Diboratio ...... m, and Synthetic Applications.

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Cobalt-Catalyzed 1,1-Diboratio ...... m, and Synthetic Applications.

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Item

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Cobalt-Catalyzed 1,1-Diboratio ...... m, and Synthetic Applications.

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Cobalt-Catalyzed 1,1-Diboratio ...... m, and Synthetic Applications.

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prefLabel

Cobalt-Catalyzed 1,1-Diboratio ...... m, and Synthetic Applications.

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Cobalt-Catalyzed 1,1-Diboratio ...... m, and Synthetic Applications.

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P1476

Cobalt-Catalyzed 1,1-Diboratio ...... m, and Synthetic Applications.

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P2093

Simon Krautwald

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P2860

Simple, efficient, and modular syntheses of polyene natural products via iterative cross-coupling

Developmental neurotoxicity of pyrethroid insecticides: critical review and future research needs

Motualevic acids A-F, antimicrobial acids from the sponge Siliquariaspongia sp

The synthesis of novel GABA uptake inhibitors. 1. Elucidation of the structure-activity studies leading to the choice of (R)-1-[4,4-bis(3-methyl-2-thienyl)-3-butenyl]-3-piperidinecarboxylic acid (tiagabine) as an anticonvulsant drug candidate.

The discovery of pyridalyl: a novel insecticidal agent for controlling lepidopterous pests.

Electronic structure of bis(imino)pyridine iron dichloride, monochloride, and neutral ligand complexes: a combined structural, spectroscopic, and computational study.

Metal vinylidenes as catalytic species in organic reactions

Boron-selective reactions as powerful tools for modular synthesis of diverse complex molecules.

A catalytic enantiotopic-group-selective Suzuki reaction for the construction of chiral organoboronates.

A convergent approach to (R)-Tiagabine by a regio- and stereocontrolled hydroiodination of alkynes.

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3868-3875

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scholarly article

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10.1021/JACS.7B00445

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English

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139

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Paul J Chirik

Máté J Bezdek

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2017-03-01T00:00:00Z

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28199104

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Béésh Łibáhí

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5697746

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Cobalt-Catalyzed 1,1-Diboration of Terminal Alkynes: Scope, Mechanism, and Synthetic Applications.

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P2860

P2860

Cobalt-Catalyzed 1,1-Diboration of Terminal Alkynes: Scope, Mechanism, and Synthetic Applications.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932