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

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

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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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Cobalt-Catalyzed Diborylation ...... ranched gem-Bis(boryl)alkanes.

@en

Cobalt-Catalyzed Diborylation ...... ranched gem-Bis(boryl)alkanes.

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type

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label

Cobalt-Catalyzed Diborylation ...... ranched gem-Bis(boryl)alkanes.

@en

Cobalt-Catalyzed Diborylation ...... ranched gem-Bis(boryl)alkanes.

@nl

prefLabel

Cobalt-Catalyzed Diborylation ...... ranched gem-Bis(boryl)alkanes.

@en

Cobalt-Catalyzed Diborylation ...... ranched gem-Bis(boryl)alkanes.

@nl

P1476

Cobalt-Catalyzed Diborylation ...... Branched gem-Bis(boryl)alkanes

@en

P2093

Shaozhong Ge

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

Wei Jie Teo

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

P2860

Synthesis of vinyl boronates from aldehydes by a practical boron-Wittig reaction.

Enantio- and Diastereoselective 1,2-Additions to α-Ketoesters with Diborylmethane and Substituted 1,1-Diborylalkanes.

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

Copper-catalyzed cross-coupling reactions of epoxides with gem-diborylmethane: access to γ-hydroxyl boronic esters.

Copper-catalyzed propargylation of diborylmethane.

Nickel-catalyzed synthesis of 1,1-diborylalkanes from terminal alkenes.

Modular, Catalytic Enantioselective Construction of Quaternary Carbon Stereocenters by Sequential Cross-Coupling Reactions.

Nonracemic allylic boronates through enantiotopic-group-selective cross-coupling of geminal bis(boronates) and vinyl halides.

Simple access to elusive α-boryl carbanions and their alkylation: an umpolung construction for organic synthesis.

Mode of Activation of Cobalt(II) Amides for Catalytic Hydrosilylation of Alkenes with Tertiary Silanes.

P304

1654-1658

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P31

scholarly article

P356

10.1002/ANIE.201710389

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

P407

English

P433

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

P478

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

P50

Shaozhong Ge

Wei Jie Teo

P577

2018-01-10T00:00:00Z

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

P698

29193560

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

P921

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