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Microwave-promoted reaction of N-(alk-1-enyl)chloroacetamides with sodium azide unexpectedly yields 1H-imidazol-5(4H)-ones. / Kantin, Grigory P.; Krasavin, Mikhail Yu.

In: Mendeleev Communications, Vol. 27, No. 1, 01.01.2017, p. 95-96.

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@article{ed4d426a6fdb4499b993a4b673bdd196,
title = "Microwave-promoted reaction of N-(alk-1-enyl)chloroacetamides with sodium azide unexpectedly yields 1H-imidazol-5(4H)-ones",
abstract = "A novel method to prepare biologically relevant 1H-imidazol-5(4H)-ones from aliphatic amines, isobutyraldehyde, chloroacetyl chloride and sodium azide under microwave irradiation has been developed.",
author = "Kantin, {Grigory P.} and Krasavin, {Mikhail Yu}",
year = "2017",
month = jan,
day = "1",
doi = "10.1016/j.mencom.2017.01.031",
language = "English",
volume = "27",
pages = "95--96",
journal = "Mendeleev Communications",
issn = "0959-9436",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Microwave-promoted reaction of N-(alk-1-enyl)chloroacetamides with sodium azide unexpectedly yields 1H-imidazol-5(4H)-ones

AU - Kantin, Grigory P.

AU - Krasavin, Mikhail Yu

PY - 2017/1/1

Y1 - 2017/1/1

N2 - A novel method to prepare biologically relevant 1H-imidazol-5(4H)-ones from aliphatic amines, isobutyraldehyde, chloroacetyl chloride and sodium azide under microwave irradiation has been developed.

AB - A novel method to prepare biologically relevant 1H-imidazol-5(4H)-ones from aliphatic amines, isobutyraldehyde, chloroacetyl chloride and sodium azide under microwave irradiation has been developed.

UR - http://www.scopus.com/inward/record.url?scp=85010430920&partnerID=8YFLogxK

UR - https://www.sciencedirect.com/science/article/abs/pii/S0959943617300317#!

U2 - 10.1016/j.mencom.2017.01.031

DO - 10.1016/j.mencom.2017.01.031

M3 - Article

AN - SCOPUS:85010430920

VL - 27

SP - 95

EP - 96

JO - Mendeleev Communications

JF - Mendeleev Communications

SN - 0959-9436

IS - 1

ER -

ID: 34634928