Published November 4, 2019
| Version v1
Journal article
H-acceptorless dehydrogenative boration and transfer boration of alkenes enabled by zirconium catalyst
Creators
- 1. State Key Laboratory for Oxo Synthesis and Selective Oxidation, Suzhou Research Institute of LICP, Lanzhou Institute of Chemical Physics (LICP), Chinese Academy of Sciences (China)
Description
The first example of an efficient and direct dehydrogenative boration of alkenes for vinyl boronate ester synthesis was achieved using a zirconium catalyst. Our methodology avoids using precious transition metals, additional hydrogen acceptors, high temperatures, and long reaction times, which were required to overcome the reducing ability of borane, to give alkyl boronate esters. Detailed mechanistic studies revealed a reversible reaction pathway and further suggested applying the zirconium complex as a "shuttle catalyst" for transfer boration, which thus sidesteps the use of relatively sensitive borane. (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)
Availability note (English)
Available from: http://dx.doi.org/10.1002/anie.201908931Additional details
Identifiers
Publishing Information
- Journal Title
- Angewandte Chemie (International Edition)
- Journal Volume
- 58
- Journal Issue
- 45
- Journal Page Range
- p. 16167-16171
- ISSN
- 1433-7851
- CODEN
- ACIEF5
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 51022792
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ALKENES; BORANES; BORATES; CATALYSTS; DEHYDROGENATION; ESTERS; ZIRCONIUM; ZIRCONIUM COMPLEXES
- Descriptors DEC
- BORON COMPOUNDS; CHEMICAL REACTIONS; COMPLEXES; ELEMENTS; HYDRIDES; HYDROCARBONS; HYDROGEN COMPOUNDS; METALS; ORGANIC COMPOUNDS; OXYGEN COMPOUNDS; TRANSITION ELEMENT COMPLEXES; TRANSITION ELEMENTS