Boron as a powerful reductant: synthesis of a stable boron-centered radical-anion radical-cation pair.
about
Powerful Bispyridinylidene Organic Reducing Agents with Iminophosphorano π-Donor Substituents.Ring expansion reactions of anti-aromatic boroles: a promising synthetic avenue to unsaturated boracycles.Formation and Reactivity of Electron-Precise B-B Single and Multiple Bonds.Generation of 1,2-azaboretidines via reduction of ADC borane adducts.Easy access to nucleophilic boron through diborane to magnesium boryl metathesis.A boron-centered radical: a potassium-crown ether stabilized boryl radical anion.Triaminotriborane(3): A Homocatenated Boron Chain Connected by B-B Multiple Bonds.The synthesis and structure of a carbene-stabilized iminocarboranyl-boron(I) compound.Crystalline boron-linked tetraaminoethylene radical cations.Increasing the Reactivity of Diborenes: Derivatization of NHC-Supported Dithienyldiborenes with Electron-Donor Groups.Dibora[2]ferrocenophane: A Carbene-Stabilized Diborene in a Strained cis-Configuration.Engineering a Small HOMO-LUMO Gap and Intramolecular C-H Borylation by Diborene/Anthracene Orbital Intercalation.Oxime Ether Radical Cations Stabilized by N-Heterocyclic Carbenes.CuOTf-mediated intramolecular diborene hydroarylation.An Isolable Diboron-Centered Diradical with a Triplet Ground State.A Radical Tricationic Rhomboid Tetraborane(4) with Four-Center, Five-Electron Bonding.Stepwise Reduction of 9,10-Bis(dimesitylboryl)anthracene.C-H addition reactivity of 2-phenylpyridine and 2,2'-bipyridine with pentaphenylborole.The Triboracyclopropenyl Dianion: The Lightest Possible Main-Group-Element Hückel π Aromatic.Dibora[2]ferrocenophan: ein carbenstabilisiertes Diboren in einer gespanntencis-Konfiguration
P2860
Q30933352-2BCED2AF-10AF-40A0-B3F0-D62BFD6AF603Q38877590-63A1B0CA-12CC-41B5-B7D4-DE892263CCBBQ39012417-6DB048E5-1154-4459-B2CD-23956F5793C3Q40989925-861F9979-C6CA-44EA-B330-B3B6F93BEE72Q41841828-7068B8C8-D0AB-4712-9E89-B0CA9B5BEF8EQ45960191-D5D8F8DD-C68F-499A-A4BC-FA660AF7D6CEQ46294364-877D4E2C-6841-4727-96DC-301C8C2301C7Q46660117-C67399AD-862C-4219-88D1-592AD2E061ACQ47122545-9C30BA46-28D0-4EB4-A9B1-CA358817F86EQ47722296-689C0E77-F876-4613-B14A-822A4F0A89E1Q48135956-0E98164C-3763-4744-84C7-033CBD10E7A3Q48158682-11B8AB21-A3E0-4E71-AF6F-2305BB2ABED4Q48308406-3C93B8DD-9604-4C6E-A7CB-54A5CB663288Q50100025-1D9D416B-80D4-427D-8FF6-154B96835196Q50182144-7A78ADB4-56BB-45B5-89AB-0F1DA2A45214Q50251553-39394F8D-3B21-4ABF-8723-647B1E8A2820Q51727788-72ECF8D5-0F8D-49FD-8019-A6E206509ECFQ52566185-393FC8D0-96F8-4EE2-8CCD-6F0FA15DC5A1Q53658462-50290379-6161-4128-BCD8-B4CF656F048FQ57903816-146B4E02-AA3A-46C3-A571-8319664E4168
P2860
Boron as a powerful reductant: synthesis of a stable boron-centered radical-anion radical-cation pair.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh
2014年學術文章
@zh-hant
name
Boron as a powerful reductant: ...... cal-anion radical-cation pair.
@en
Boron as a powerful reductant: ...... cal-anion radical-cation pair.
@nl
type
label
Boron as a powerful reductant: ...... cal-anion radical-cation pair.
@en
Boron as a powerful reductant: ...... cal-anion radical-cation pair.
@nl
prefLabel
Boron as a powerful reductant: ...... cal-anion radical-cation pair.
@en
Boron as a powerful reductant: ...... cal-anion radical-cation pair.
@nl
P2093
P2860
P356
P1476
Boron as a powerful reductant: ...... ical-anion radical-cation pair
@en
P2093
Alexander Damme
Christian Hörl
Philipp Bissinger
Thomas Kupfer
P2860
P304
P356
10.1002/ANIE.201409513
P407
P577
2014-11-11T00:00:00Z