Published August 3, 2020
| Version v1
Journal article
as a synthon for the generation of boron-centered carbamate and carboxylate isosteres
- 1. Department of Chemistry, University of Bath, Bath, BA2 7AY (United Kingdom)
Description
Oxoborane carbamate and carboxylate analogues result from the in situ trapping of produced by elimination of 2,3-dimethyl-2-butene from a pinacolatoboryl anion. (© 2020 The Authors. Published by Wiley-VCH Verlag GmbH and Co. KGaA.)
Additional details
Identifiers
Publishing Information
- Journal Title
- Angewandte Chemie (International Edition)
- Journal Volume
- 59
- Journal Issue
- 32
- Journal Page Range
- p. 13628-13632
- ISSN
- 1433-7851
- CODEN
- ACIEF5
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 51107953
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S36: MATERIALS SCIENCE;
- Descriptors DEI
- ANIONS; BOND ANGLE; BOND LENGTHS; BORANES; BUTENES; CARBAMATES; CARBENES; CHEMISTRY; DENSITY FUNCTIONAL METHOD; MAGNESIUM COMPLEXES; NMR SPECTRA; ORGANIC BORON COMPOUNDS; SYNTHESIS; X-RAY DIFFRACTION
- Descriptors DEC
- ALKALINE EARTH METAL COMPLEXES; ALKENES; BORON COMPOUNDS; CALCULATION METHODS; CARBONIC ACID DERIVATIVES; CARBOXYLIC ACID SALTS; CHARGED PARTICLES; COHERENT SCATTERING; COMPLEXES; DIFFRACTION; DIMENSIONS; HYDRIDES; HYDROCARBONS; HYDROGEN COMPOUNDS; IONS; LENGTH; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; RADICALS; SCATTERING; SPECTRA; VARIATIONAL METHODS