Repository logo

Infoscience

  • English
  • French
Log In
Logo EPFL, École polytechnique fédérale de Lausanne

Infoscience

  • English
  • French
Log In
  1. Home
  2. Academic and Research Output
  3. Journal articles
  4. Cobalt-Catalyzed Hydroazidation of Olefins: Convenient Access to Alkyl Azides
 
research article

Cobalt-Catalyzed Hydroazidation of Olefins: Convenient Access to Alkyl Azides

Waser, Jerome  
•
Nambu, Hisanori
•
Carreira, Erick M.
2005
Journal of the American Chemical Society

Conversion of unactivated olefins to azides was achieved with high Markovnikov selectivity for a broad range of alkenes by using 6 mol % Co(BF4).6H2O and ligand I, with 3 equiv of tosyl azide as the nitrogen source and simple silanes (e.g., PhSiH3, tetramethyldisiloxane). [on SciFinder (R)]

  • Details
  • Metrics
Type
research article
DOI
10.1021/ja052164r
Author(s)
Waser, Jerome  
Nambu, Hisanori
Carreira, Erick M.
Date Issued

2005

Published in
Journal of the American Chemical Society
Volume

127

Issue

23

Start page

8294

End page

8295

Subjects

Alkenes Role: RCT (Reactant)

•

RACT (Reactant or reagent) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins); Azides Role: SPN (Synthetic preparation)

•

PREP (Preparation) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins)

•

alkyl azide prepn cobalt catalysis hydroazidation olefin

Note

CAN 143:133069

23-5

Aliphatic Compounds

Laboratorium fuer Organische Chemie,ETH Hoenggerberg,Zurich,Switz.

Journal

written in English.

15684-35-2 (Cobalt bis(tetrafluoroborate) hexahydrate); 15684-35-2D (Cobalt bis(tetrafluoroborate) hexahydrate); 858344-69-1D Role: CAT (Catalyst use), USES (Uses) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins); 858344-69-1P Role: CAT (Catalyst use), RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), USES (Uses), RACT (Reactant or reagent) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins); 6147-53-1; 10026-22-9 (Cobalt dinitrate hexahydrate) Role: CAT (Catalyst use), RGT (Reagent), USES (Uses), RACT (Reactant or reagent) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins); 704900-51-6P; 858671-40-6P; 858671-46-2P Role: CAT (Catalyst use), SPN (Synthetic preparation), PREP (Preparation), USES (Uses) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins); 62-57-7 (2-Aminoisobutyric acid); 90-02-8 (Salicylaldehyde); 94-59-7; 98-86-2 (Acetophenone); 100-39-0 (Benzyl bromide); 106-95-6 (Allyl bromide); 107-18-6 (Allyl alcohol); 127-91-3; 513-42-8 (Methallyl alcohol); 536-74-3 (Phenylacetylene); 556-82-1 (3-Methyl-2-butenol); 563-47-3 (Methallyl chloride); 591-80-0 (4-Pentenoic acid); 627-27-0 (3-Buten-1-ol); 768-56-9; 939-26-4 (2-(Bromomethyl)naphthalene); 941-55-9 (Tosyl azide); 1730-25-2 (Allylmagnesium bromide); 3060-50-2 (alpha,alpha-Diphenylglycine); 14593-43-2; 37942-07-7 (3,5-Di-tert-butylsalicylaldehyde); 58479-61-1 (tert-Butyldiphenylsilyl chloride); 75031-69-5 (Butoxy-tert-butyldiphenylsilane); 221313-63-9 (Propoxy-tert-butyldiphenylsilane); 858344-71-5 (3-(Diphenylphosphinoyl)-3-methyl-5-phenylpentan-2-ol) Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins); 2489-89-6P; 3240-29-7P; 6683-51-8P; 72485-49-5P; 105966-43-6P; 113882-48-7P; 135006-32-5P; 136787-49-0P; 188263-82-3P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins); 694-53-1 (Phenylsilane); 30110-74-8 (Tetramethyldisiloxane) Role: RGT (Reagent), RACT (Reactant or reagent) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins); 104-51-8P (1-Phenylbutane); 22374-89-6P; 32366-28-2P; 58977-25-6P; 166327-12-4P; 475152-60-4P; 858344-60-2P; 858344-61-3P; 858344-62-4P; 858344-63-5P; 858344-64-6P; 858344-65-7P; 858344-66-8P; 858344-67-9P; 858344-68-0P; 858344-70-4P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of alkyl azides via cobalt-catalyzed hydroazidation of olefins)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LCSO  
Available on Infoscience
December 17, 2007
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/15789
Logo EPFL, École polytechnique fédérale de Lausanne
  • Contact
  • infoscience@epfl.ch

  • Follow us on Facebook
  • Follow us on Instagram
  • Follow us on LinkedIn
  • Follow us on X
  • Follow us on Youtube
AccessibilityLegal noticePrivacy policyCookie settingsEnd User AgreementGet helpFeedback

Infoscience is a service managed and provided by the Library and IT Services of EPFL. © EPFL, tous droits réservés