An Efficient One-Pot Conversion of Alkyl Bromides into Imines via the Staudinger Reaction

VANĚK, Petr and Petr KLÁN. An Efficient One-Pot Conversion of Alkyl Bromides into Imines via the Staudinger Reaction. Synthetic Communications. New York: Marcel Dekker, 2000, vol. 30, No 8, p. 1503-1507. ISSN 0039-7911.

Basic information

Original name

An Efficient One-Pot Conversion of Alkyl Bromides into Imines via the Staudinger Reaction

Authors

VANĚK, Petr and Petr KLÁN (203 Czech Republic, guarantor)

Edition

Synthetic Communications, New York, Marcel Dekker, 2000, 0039-7911

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Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

10401 Organic chemistry

Country of publisher

United States of America

Confidentiality degree

není předmětem státního či obchodního tajemství

Impact factor

Impact factor: 0.828

RIV identification code

RIV/00216224:14310/00:00002181

Organization unit

Faculty of Science

UT WoS

000086376200018

Keywords (in Czech)

fotochemie

Keywords in English

photochemistry

Tags

Photochemistry

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Abstract

V originále

A new one-pot procedure for transforming primary alkyl bromides into the corresponding imines via the Staudinger reaction has been developed. Acetonitrile was found to be an excellent solvent for azidation as well as the reaction of organic azide with triphenylphosphine and a carbonyl compound.

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Links

MSM 143100011, plan (intention)

Name: Struktura a vazebné poměry, vlastnosti a analýza syntetických a přírodních molekulových ansamblů Investor: Ministry of Education, Youth and Sports of the CR, Structure and character of bonding, properties and analysis of synthetic and natural molecular ensembles