about
Hydrogenations at room temperature and atmospheric pressure with mesoionic carbene-stabilized borenium catalysts.Facile Arylation of Four-Coordinate Boron Halides by Borenium Cation Mediated Boro-desilylation and -destannylation.Catalyst-Free Synthesis of Borylated Lactones from Esters via Electrophilic Oxyboration.The broadening reach of frustrated Lewis pair chemistry.Versatile coordination of a reactive P,N-ligand toward boron, aluminum and gallium and interconversion reactivity.Boron-mediated sequential alkyne insertion and C-C coupling reactions affording extended π-conjugated molecules.Carboberyllation: addition of organoberyllium species to alkenes and alkynes. A comparison with carboboration.Chiral carbene-borane adducts: precursors for borenium catalysts for asymmetric FLP hydrogenations.Diverse reactivity of borenium cations with >N-H compounds.Design and reactions of a carbon Lewis base/boron Lewis acid frustrated Lewis pair.Hydroboration of Phosphaalkynes by HB(C6 F5 )2.Formation of an Isolable Divinylborinium Ion through Twofold 1,2-Carboboration between a Diarylborinium Ion and Diphenylacetylene.A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.N-Heterocycle-Ligated Borocations as Highly Tunable Carbon Lewis Acids.Complete reductive cleavage of CO facilitated by highly electrophilic borocations.A Stable but Highly Reactive Phosphine-Coordinated Borenium: Metal-free Dihydrogen Activation and Alkyne 1,2-Carboboration.The Propargyl Rearrangement to Functionalised Allyl-Boron and Borocation Compounds.Transition Metal-Free 1,2-Carboboration of Unactivated Alkenes.Formation of an Isolable Divinylborinium Ion through Twofold 1,2-Carboboration between a Diarylborinium Ion and Diphenylacetylene
P2860
Q33463906-587EAE7C-94C1-46CF-B8FE-A1B7DFDAC14DQ36761426-08992EA4-EAA4-466F-B095-F8B2485F66EAQ38647474-3F5398A9-5F08-49D8-9792-DB436E2BFE89Q38784422-7B243F21-2818-4719-957A-4C9ABE1878FDQ39681205-756E687A-5AB9-4BCC-BC87-461BCADBEB19Q41107827-6DC96723-DA1C-499A-8B99-094547349616Q46362032-B73D2297-233E-4E94-BD90-1FF5C173D3C6Q46522391-3428EFEB-A1F3-4815-A188-F6C492D74025Q46526225-6C2478F3-845B-4615-B95E-71AAABAE9CDBQ47753514-63C03AC2-48E0-47DA-A226-463080F6A009Q48175739-9F765010-F321-4EE9-B93D-8DA2A2B69162Q48330093-9B07E34E-78B7-4F17-9C17-23C898B870DCQ49955997-2C7EB75B-0394-48B1-922D-74A119CB7F7AQ50074097-E7665E6C-99CC-484F-BD17-721C9F9DF929Q52937660-5AC7BEBB-E617-44F3-8BE0-4F9463AC6317Q52956836-809806AD-EC7D-420B-A62D-667441B807FCQ52965867-52ECC4C1-8164-4B73-9ED6-4D0D57ECA7FDQ55288423-4DB82E28-DA61-4351-BB79-B12285D44367Q57702663-F57A08D7-F8CB-40A7-A686-9CCB8B55DC2D
P2860
description
2014 nî lūn-bûn
@nan
2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
syn-1,2-carboboration of alkynes with borenium cations.
@ast
syn-1,2-carboboration of alkynes with borenium cations.
@en
syn-1,2-carboboration of alkynes with borenium cations.
@nl
type
label
syn-1,2-carboboration of alkynes with borenium cations.
@ast
syn-1,2-carboboration of alkynes with borenium cations.
@en
syn-1,2-carboboration of alkynes with borenium cations.
@nl
prefLabel
syn-1,2-carboboration of alkynes with borenium cations.
@ast
syn-1,2-carboboration of alkynes with borenium cations.
@en
syn-1,2-carboboration of alkynes with borenium cations.
@nl
P2860
P356
P1476
syn-1,2-carboboration of alkynes with borenium cations.
@en
P2860
P304
12874-12880
P356
10.1002/CHEM.201403614
P407
P577
2014-08-19T00:00:00Z