Research output: Contribution to journal › Article › peer-review
Unprecedented 1,3-dipolar cycloaddition of azomethine ylides derived from difluorocarbene and imines to carbonyl compounds. - Synthesis of oxazolidine derivatives. / Novikov, Mikhail S.; Khlebnikov, Alexander F.; Krebs, Adolf; Kostikov, Rafael R.
In: European Journal of Organic Chemistry, No. 1, 01.1998, p. 133-137.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Unprecedented 1,3-dipolar cycloaddition of azomethine ylides derived from difluorocarbene and imines to carbonyl compounds. - Synthesis of oxazolidine derivatives
AU - Novikov, Mikhail S.
AU - Khlebnikov, Alexander F.
AU - Krebs, Adolf
AU - Kostikov, Rafael R.
N1 - Copyright: Copyright 2020 Elsevier B.V., All rights reserved.
PY - 1998/1
Y1 - 1998/1
N2 - Iminiodifluoromethanides generated by the reaction of difluorocarbene with benzaldehyde and benzophenone imines undergo regioselective 1,3-dipolar cycloaddition to aldehydes to give oxazolidine derivatives.
AB - Iminiodifluoromethanides generated by the reaction of difluorocarbene with benzaldehyde and benzophenone imines undergo regioselective 1,3-dipolar cycloaddition to aldehydes to give oxazolidine derivatives.
KW - Azomethine ylides
KW - Cycloadditions
KW - Difluorocarbene
KW - Heterocycles
KW - Oxazolidines
UR - http://www.scopus.com/inward/record.url?scp=0002401823&partnerID=8YFLogxK
U2 - 10.1002/(sici)1099-0690(199801)1998:1<133::aid-ejoc133>3.0.co;2-u
DO - 10.1002/(sici)1099-0690(199801)1998:1<133::aid-ejoc133>3.0.co;2-u
M3 - Article
SP - 133
EP - 137
JO - European Journal of Organic Chemistry
JF - European Journal of Organic Chemistry
SN - 1434-193X
IS - 1
ER -
ID: 5057194