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  4. Alkene hydrazination: Catalytic hydrohydrazination of a wide range of alkenes with a simple Mn complex
 
research article

Alkene hydrazination: Catalytic hydrohydrazination of a wide range of alkenes with a simple Mn complex

Waser, Jerome  
•
Carreira, Erick M.
2004
Angewandte Chemie International Edition

Enhanced activity, lower catalyst loading, shorter reaction time, and expanded substrate scope are the advantages of [Mn(dpm)3] over Co catalysts in the hydrohydrazination reaction of alkenes. Thus, sterically hindered alkenes, including tetrasubstituted alkenes, can now also readily undergo this reaction. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1002/anie.200460811
Author(s)
Waser, Jerome  
Carreira, Erick M.
Date Issued

2004

Publisher

Wiley-VCH Verlag GmbH

Published in
Angewandte Chemie International Edition
Volume

43

Issue

31

Start page

4099

End page

4102

Subjects

Addition reaction; Addition reaction catalysts (manganese-catalyzed hydrohydrazination of alkenes); Alkenes; Cycloalkenes Role: RCT (Reactant)

•

RACT (Reactant or reagent) (manganese-catalyzed hydrohydrazination of alkenes)

•

manganese catalyst hydrohydrazination alkene

Note

CAN 141:331638

21-2

General Organic Chemistry

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

Journal

written in English.

704900-51-6P Role: CAT (Catalyst use), SPN (Synthetic preparation), PREP (Preparation), USES (Uses) (cobalt- or manganese-catalyzed hydrohydrazination of alkenes); 62-57-7 (2-Aminoisobutyric acid); 90-02-8 (Salicylaldehyde) Role: RCT (Reactant), RACT (Reactant or reagent) (cobalt- or manganese-catalyzed hydrohydrazination of alkenes); 773882-01-2P Role: BYP (Byproduct), SPN (Synthetic preparation), PREP (Preparation) (manganese-catalyzed hydrohydrazination of alkenes); 14324-99-3P Role: CAT (Catalyst use), SPN (Synthetic preparation), PREP (Preparation), USES (Uses) (manganese-catalyzed hydrohydrazination of alkenes); 67-64-1 (Acetone); 91-20-3 (Naphthalene); 98-86-2 (Acetophenone); 103-26-4 (Methyl cinnamate); 103-36-6; 110-83-8 (Cyclohexene); 142-29-0 (Cyclopentene); 498-66-8 (Norbornene); 563-79-1 (2,3-Dimethyl-2-butene); 583-60-8 (2-Methylcyclohexanone); 623-70-1 (Ethyl (E)-Crotonate); 627-27-0 (3-Buten-1-ol); 637-50-3 (1-Propenylbenzene); 763-29-1; 768-56-9 (Allylbenzene); 870-50-8 (Di-tert-butyl azodicarboxylate); 931-88-4 (Cyclooctene); 1118-71-4; 4786-20-3 (2-Butenenitrile); 6117-91-5 (2-Buten-1-ol); 13269-52-8 (trans-3-Hexene) Role: RCT (Reactant), RACT (Reactant or reagent) (manganese-catalyzed hydrohydrazination of alkenes); 493-03-8P; 769-57-3P; 1674-10-8P (1,2-Dimethylcyclohexene); 5402-29-9P (1,2-Dimethylcyclohexanol) Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (manganese-catalyzed hydrohydrazination of alkenes); 180137-93-3P; 345210-67-5P; 704899-91-2P; 704900-21-0P; 704900-28-7P; 704900-42-5P; 704900-46-9P; 704900-48-1P; 704900-57-2P; 773882-00-1P; 773882-02-3P; 773882-03-4P; 773882-04-5P; 773882-05-6P; 773882-06-7P; 773882-07-8P; 773882-08-9P; 773882-09-0P Role: SPN (Synthetic preparation), PREP (Preparation) (manganese-catalyzed hydrohydrazination of alkenes); 789-25-3 (Triphenylsilane); 9004-73-3 (Poly(methylhydrosiloxane); 49718-23-2 Role: RGT (Reagent), RACT (Reactant or reagent) (reductant; manganese-catalyzed hydrohydrazination of alkenes)

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/20.500.14299/15788
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