Literature DB >> 25754121

Synthesis and characterization of tricarbastannatranes and their reactivity in B(C6F5)3-promoted conjugate additions.

Azadeh Kavoosi1, Eric Fillion.   

Abstract

The synthesis and characterization of a series of tricarbastannatranes, in the solid state and in solution, are described. The structures of the complexes [N(CH2 CH2 CH2 )3 Sn](BF4 ), [N(CH2 CH2 CH2 )3 Sn](SbF6 ), [N(CH2 CH2 CH2 )3 Sn]4 [(SbF6 )3 Cl], and [(N(CH2 CH2 CH2 )3 Sn)2 OH][MeB(C6 F5 )3 ] were determined by X-ray crystallography. Furthermore, the B(C6 F5 )3 -promoted conjugate addition of alkyl-tricarbastannatranes to benzylidene derivatives of Meldrum's acid was investigated, and detailed mechanistic studies are presented.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Lewis acid; Michael addition; boron; reaction mechanisms; tin

Year:  2015        PMID: 25754121     DOI: 10.1002/anie.201500983

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


  3 in total

1.  Stereospecific Palladium-Catalyzed Acylation of Enantioenriched Alkylcarbastannatranes: A General Alternative to Asymmetric Enolate Reactions.

Authors:  Chao-Yuan Wang; Glenn Ralph; Joseph Derosa; Mark R Biscoe
Journal:  Angew Chem Int Ed Engl       Date:  2016-12-16       Impact factor: 15.336

2.  Stereospecific Electrophilic Fluorination of Alkylcarbastannatrane Reagents.

Authors:  Xinghua Ma; Mohamed Diane; Glenn Ralph; Christine Chen; Mark R Biscoe
Journal:  Angew Chem Int Ed Engl       Date:  2017-09-04       Impact factor: 15.336

3.  Preparation of Enantioenriched Alkylcarbastannatranes via Nucleophilic Inversion of Alkyl Mesylates for Use in Stereospecific Cross-Coupling Reactions.

Authors:  Glenn Ralph; Mark R Biscoe
Journal:  Organometallics       Date:  2019-09-03       Impact factor: 3.876

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.