Literature DB >> 32401402

[BO2 ]- as a Synthon for the Generation of Boron-Centered Carbamate and Carboxylate Isosteres.

Anne-Frédérique Pécharman1, Michael S Hill1, Claire L McMullin1, Mary F Mahon1.   

Abstract

Oxoborane carbamate and carboxylate analogues result from the in situ trapping of [BO2 ]- produced by elimination of 2,3-dimethyl-2-butene from a pinacolatoboryl anion.
© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

Entities:  

Keywords:  boryl; density functional theory; dioxoborane; magnesium; main group chemistry

Year:  2020        PMID: 32401402     DOI: 10.1002/anie.202005674

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  A Terphenyl Supported Dioxophosphorane Dimer: the Light Congener of Lawesson's and Woollins' Reagents.

Authors:  Laura E English; Aleksandra Pajak; Claire L McMullin; John P Lowe; Mary F Mahon; David J Liptrot
Journal:  Chemistry       Date:  2022-04-06       Impact factor: 5.020

Review 2.  Acid-Base Free Main Group Carbonyl Analogues.

Authors:  Ying Kai Loh; Simon Aldridge
Journal:  Angew Chem Int Ed Engl       Date:  2020-10-19       Impact factor: 15.336

  2 in total

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