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Facile Synthesis of Cyanide and Isocyanides from CO.
Xu, Maotong; Kooij, Bastiaan; Wang, Tongtong; Lin, Jack H; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Afiliação
  • Xu M; Department of Chemistry, University of Toronto, 80 St. George St., Toronto, Ontario, M5S3H6, Canada.
  • Kooij B; Department of Chemistry, University of Toronto, 80 St. George St., Toronto, Ontario, M5S3H6, Canada.
  • Wang T; Van't Hoff Institute for Molecular Sciences, University of Amsterdam, 1090 GD, Amsterdam, The Netherlands.
  • Lin JH; Department of Chemistry, University of Toronto, 80 St. George St., Toronto, Ontario, M5S3H6, Canada.
  • Qu ZW; School of Chemistry, Faculty of Chemical, Environmental and Biological Science and Technology, Dalian University of Technology, Dalian, 116023, China.
  • Grimme S; Department of Chemistry, University of Toronto, 80 St. George St., Toronto, Ontario, M5S3H6, Canada.
  • Stephan DW; Mulliken Center for Theoretical Chemistry, Institut für Physikalische und Theoretische Chemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Beringstrasse 4, 53115, Bonn, Germany.
Angew Chem Int Ed Engl ; 60(31): 16965-16969, 2021 Jul 26.
Article em En | MEDLINE | ID: mdl-34004079
ABSTRACT
The reaction of K[N(SiMe3 )2 ] with 13 CO proceeds in C6 D6 or THF affording K13 CN and O(SiMe3 )2 under mild conditions as confirmed by crystallographic characterization of K(18-crown-6)CN. Similarly reaction of the alkali metal amides, M[N(SiR3 )R'] (M=Li, K; R=Ph, Me; R'=alkyl, aryl) provides the corresponding 13 C labeled isocyanide RN13 C and MOSiR3 , generally in high yields. In some instances, the use of the sterically bulky Ph3 Si-substituent is required to preclude 1,2-silyl migration affording the silylcarbamoyl salt M[Me3 SiC(O)NR']. These reactions have been used to obtain 19 examples of 13 C labelled isocyanides, and several examples of gram scale reactions are reported. The mechanism of the reactions is probed via reliable DFT calculations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article