ChemInform Abstract: Simple and Efficient One-Pot Synthesis of Nitriles from Amides and Oximes Using in situ-Generated Burgess-Type Reagent

ChemInform Abstract: Simple and Efficient One-Pot Synthesis of Nitriles from Amides and Oximes Using in situ-Generated Burgess-Type Reagent

The Burgess‐type reagent is generated in situ from chlorosulfonyl isocyanate and two equivalents 1‐(2‐hydroxyethyl)piperidine in dry methylene chloride at 0‐5 °C.

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Veröffentlicht in:ChemInform 2012-07, Vol.43 (28), p.no-no
Hauptverfasser: Rappai, John P., Karthikeyan, Jayakumar, Prathapan, Sreedharan, Unnikrishnan, Perupparampil A.
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Sprache:eng
Schlagworte:
cyanation
cyanation, nitrile formation
nitrile formation
nitriles (benzene compounds)
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container_end_page no
container_issue 28
container_start_page no
container_title ChemInform
container_volume 43
creator Rappai, John P.
Karthikeyan, Jayakumar
Prathapan, Sreedharan
Unnikrishnan, Perupparampil A.
description The Burgess‐type reagent is generated in situ from chlorosulfonyl isocyanate and two equivalents 1‐(2‐hydroxyethyl)piperidine in dry methylene chloride at 0‐5 °C.
doi_str_mv 10.1002/chin.201228079
format Article
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source Wiley Online Library Journals Frontfile Complete
subjects cyanation
cyanation, nitrile formation
nitrile formation
nitriles (benzene compounds)
title ChemInform Abstract: Simple and Efficient One-Pot Synthesis of Nitriles from Amides and Oximes Using in situ-Generated Burgess-Type Reagent
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