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


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.

SUBMITTER: Pecharman AF 

PROVIDER: S-EPMC7496551 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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[BO<sub>2</sub> ]<sup>-</sup> as a Synthon for the Generation of Boron-Centered Carbamate and Carboxylate Isosteres.

Pécharman Anne-Frédérique AF   Hill Michael S MS   McMullin Claire L CL   Mahon Mary F MF  

Angewandte Chemie (International ed. in English) 20200604 32


Oxoborane carbamate and carboxylate analogues result from the in situ trapping of [BO<sub>2</sub> ]<sup>-</sup> produced by elimination of 2,3-dimethyl-2-butene from a pinacolatoboryl anion. ...[more]

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