
Boron-Chem-Research
@boron_chemistry
Latest research in organoboron chemistry
ID: 809101410558242816
14-12-2016 18:23:03
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Boronate Formation-Triggered AzideāAlkyne Cycloaddition (J Org Chem/Org Lett): pubs.acs.org/doi/10.1021/ac⦠(ęę©åå¦ćå¦ć¶äŗŗ).


Titanium-Mediated Rearrangement of Bis(alkynyl)boranes: BāC Activation vs CāH Activation (Angewandte Chemie): onlinelibrary.wiley.com/doi/10.1002/an⦠(The Ye Group)


Selective CāH Borylation of Polyaromatic Compounds Enabled by Metal-Arene Ļ-Complexation (J. Am. Chem. Soc.): pubs.acs.org/doi/10.1021/jaā¦.


Synthesis of strained, air-stable boracycles via boronācarbon-centred diradicals (Nature Chemistry): nature.com/articles/s4155⦠(Yangjian Quan (QUAN LAB)).


Synthesis of Polysubstitued Naphthalenes via Metal-free Borylative Cyclization of o-Alkynylstyrenes (Adv. Synth. & Catal.): advanced.onlinelibrary.wiley.com/doi/abs/10.100ā¦.


C=O and C=S bond activation by an annulated 1,4,2-diazaborole (DaltonTransactions): pubs.rsc.org/en/content/art⦠(Pranckevicius Group).


The Importance of Atomic Charges for Predicting Site-Selective Ir-, Ru-, and Rh-Catalyzed CāH Borylations (J Org Chem/Org Lett): pubs.acs.org/doi/10.1021/ac⦠(LambertGroupODU).


Light- and Heat-Responsive Frustrated Lewis Pair Enables On-Demand Fixation of Ethylene (J. Am. Chem. Soc.): pubs.acs.org/doi/abs/10.102ā¦.



Gallium-catalyzed recycling of silicone waste with boron trichloride to yield key chlorosilanes (Science Magazine): science.org/doi/abs/10.112⦠(Steven Roldan (ć¹ćć£ć¼ć“ć³))

Regioselective, Lewis Acid-Catalyzed Ring-Openings of 2,3-Aziridyl Alcohols with Azoles (J Org Chem/Org Lett): pubs.acs.org/doi/abs/10.102ā¦.


BBr3-Mediated ortho CāH Borylation of Benzamides (J Org Chem/Org Lett): pubs.acs.org/doi/10.1021/acā¦.


The connection between hydride affinity and local electrophilicity: a key factor in designing frustrated Lewis pairs for reversible H2 activation (DaltonTransactions): pubs.rsc.org/en/content/artā¦.


A Boron-Doped Triple Helicene: Synthesis, Structure, and Optoelectronic Properties (ScienceDirect): sciencedirect.com/science/articlā¦


Base Mediated 1,2-Carboboration: Direct Access to Multisubstituted Alkenyl and Alkylboronates (J Org Chem/Org Lett): pubs.acs.org/doi/10.1021/ac⦠(Shubhankar Bose).


Xanthopinacol Boronate: A Robust, Photochemically Assembled and Cleavable Boronic Ester for Orthogonal Chemistry (Angewandte Chemie): onlinelibrary.wiley.com/doi/10.1002/an⦠Hall Research Group at UAlberta).



[B(O2C2(CF3)4)2]ā ([FPB]ā): Repurposing This Weakly Coordinating Anion for Solid-State Molecular Organometallic (SMOM) Chemistry (Organometallics): pubs.acs.org/doi/10.1021/ac⦠(Andrew Weller).
![Boron-Chem-Research (@boron_chemistry) on Twitter photo [B(O2C2(CF3)4)2]ā ([FPB]ā): Repurposing This Weakly Coordinating Anion for Solid-State Molecular Organometallic (SMOM) Chemistry (<a href="/Orgmet_ACS/">Organometallics</a>): pubs.acs.org/doi/10.1021/ac⦠(<a href="/WellerYorkChem/">Andrew Weller</a>). [B(O2C2(CF3)4)2]ā ([FPB]ā): Repurposing This Weakly Coordinating Anion for Solid-State Molecular Organometallic (SMOM) Chemistry (<a href="/Orgmet_ACS/">Organometallics</a>): pubs.acs.org/doi/10.1021/ac⦠(<a href="/WellerYorkChem/">Andrew Weller</a>).](https://pbs.twimg.com/media/GqOgV2bWQAA7soN.jpg)

Development and enantioselective synthesis of spirobiindoles via Rh-catalyzed asymmetric arylation-spirocyclization sequence Boron-Chem-Research doi.org/10.1016/j.ccleā¦


Alkali metal salts of 1,2,3-benzodiazaborines: platforms for late-stage N-functionalization and metal complexation (The Braunschweig Group): pubs.rsc.org/en/content/art⦠(Chemical Science).
