Substrate-Assisted, Transition-Metal-Free Diboration of Alkynamides with Mixed Diboron: Regio- and Stereoselective Access to trans-1,2-Vinyldiboronates.

about

Brønsted Base-Mediated Regio- and Stereoselective trans-Silaboration of Propargylamides: Access to 1,2-Vinylborasilanes.Alkylideneborate zwitterions and C-C coupling by atypical diboration of electron-rich alkynes.

P2860

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P2860

Substrate-Assisted, Transition-Metal-Free Diboration of Alkynamides with Mixed Diboron: Regio- and Stereoselective Access to trans-1,2-Vinyldiboronates.

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http://www.wikidata.org/entity/Q45056249

description

2017 nî lūn-bûn

@nan

2017年の論文

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2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Substrate-Assisted, Transition ...... to trans-1,2-Vinyldiboronates.

@en

Substrate-Assisted, Transition ...... to trans-1,2-Vinyldiboronates.

@nl

type

Item

label

Substrate-Assisted, Transition ...... to trans-1,2-Vinyldiboronates.

@en

Substrate-Assisted, Transition ...... to trans-1,2-Vinyldiboronates.

@nl

prefLabel

Substrate-Assisted, Transition ...... to trans-1,2-Vinyldiboronates.

@en

Substrate-Assisted, Transition ...... to trans-1,2-Vinyldiboronates.

@nl

P1476

Substrate-Assisted, Transition ...... to trans-1,2-Vinyldiboronates.

@en

P2093

Astha Verma

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

Carla Slebodnick

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

Fu Yao

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

Haizhu Yu

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

Russell F Snead

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

Yinuo Yang

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

Yumin Dai

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

P2860

Unexpected copper(II) catalysis: catalytic amine base promoted β-borylation of α,β-unsaturated carbonyl compounds in water.

Transition-metal-free B-B and B-interelement reactions with organic molecules.

Enantioselective conjugate silyl additions to cyclic and acyclic unsaturated carbonyls catalyzed by Cu complexes of chiral N-heterocyclic carbenes

Mechanism of NHC-Catalyzed Conjugate Additions of Diboron and Borosilane Reagents to α,β-Unsaturated Carbonyl Compounds.

Metal-free catalytic enantioselective C-B bond formation: (pinacolato)boron conjugate additions to α,β-unsaturated ketones, esters, Weinreb amides, and aldehydes promoted by chiral N-heterocyclic carbenes.

Hydroxyl-directed stereoselective diboration of alkenes.

Efficient C-B bond formation promoted by N-heterocyclic carbenes: synthesis of tertiary and quaternary B-substituted carbons through metal-free catalytic boron conjugate additions to cyclic and acyclic alpha,beta-unsaturated carbonyls.

Hydroxyl-Directed Cross-Coupling: A Scalable Synthesis of Debromohamigeran E and Other Targets of Interest.

Activation of diboron reagents with Brønsted bases and alcohols: an experimental and theoretical perspective of the organocatalytic boron conjugate addition reaction.

Chemo-, Regio-, and Stereoselective Copper(II)-Catalyzed Boron Addition to Acetylenic Esters and Amides in Aqueous Media.

P304

5111-5115

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P31

scholarly article

P356

10.1002/ANIE.201700946

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P407

English

P433

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

P478

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

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Webster L Santos

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2017-03-29T00:00:00Z

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P698

28371182

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P921

Auergungsmetal

stereoselectivity

Substrate-Assisted, Transition-Metal-Free Diboration of Alkynamides with Mixed Diboron: Regio- and Stereoselective Access to trans-1,2-Vinyldiboronates.

about

P2860

P2860

Substrate-Assisted, Transition-Metal-Free Diboration of Alkynamides with Mixed Diboron: Regio- and Stereoselective Access to trans-1,2-Vinyldiboronates.

description

name

type

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921