New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives-Reference-Cited by-同舟云学术

New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives

Published:2016 Issue:27 Volume:52 Page:4898-4901
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Arnold Nicole¹²³⁴,Braunschweig Holger¹²³⁴,Damme Alexander¹²³⁴,Dewhurst Rian D.¹²³⁴,Pentecost Leanne⁵⁶⁷⁸⁹,Radacki Krzysztof¹²³⁴,Stellwag-Konertz Sascha¹²³⁴,Thiess Torsten¹²³⁴,Trumpp Alexandra¹²³⁴,Vargas Alfredo⁵⁶⁷⁸⁹

Affiliation:

1. Institut für Anorganische Chemie

2. Julius-Maximilians-Universität Würzburg

3. 97074 Würzburg

4. Germany

5. Department of Chemistry

6. School of Life Sciences

7. University of Sussex

8. Sussex

9. UK

Abstract

Two surprising new outcomes of the reaction of Lewis bases with dihalodiboranes(4) are presented.

Funder

Engineering and Physical Sciences Research Council

University Of Sussex

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CC/C6CC01493C

Reference45 articles.

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3. C−H Activation for the Construction of C−B Bonds

4. Borylation and Silylation of C–H Bonds: A Platform for Diverse C–H Bond Functionalizations

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