Research output: Contribution to journal › Article › peer-review
Fluorination of α-diazo-γ-lactams with the Olah reagent. / Kazantsev, Alexander; Zhukovsky, Daniil; Bubyrev, Andrey; Dar'in, Dmitry; Krasavin, Mikhail.
In: Tetrahedron Letters, Vol. 69, 152969, 13.04.2021.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Fluorination of α-diazo-γ-lactams with the Olah reagent
AU - Kazantsev, Alexander
AU - Zhukovsky, Daniil
AU - Bubyrev, Andrey
AU - Dar'in, Dmitry
AU - Krasavin, Mikhail
N1 - Funding Information: This research was supported by the Russian Foundation for Basic Research (project grant 19-33-90016). We are grateful to the Research Centre for Magnetic Resonance and the Centre for Chemical Analysis and Materials Research of Saint Petersburg State University Research Park for the analytical data. Publisher Copyright: © 2021 Elsevier Ltd Copyright: Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/4/13
Y1 - 2021/4/13
N2 - A series of N-aryl α-fluoro-γ-lactams were successfully prepared by hydrofluorination of diazo counterparts with the Olah reagent in moderate yields. This approach was also applied to bromofluorination with N-bromosuccinimide as electrophilic bromine source.
AB - A series of N-aryl α-fluoro-γ-lactams were successfully prepared by hydrofluorination of diazo counterparts with the Olah reagent in moderate yields. This approach was also applied to bromofluorination with N-bromosuccinimide as electrophilic bromine source.
KW - Diazo compounds
KW - N-aryl 2-pyrrolidones
KW - The Olah reagent
KW - α-Fluorination of carbonyl compounds
KW - alpha-Fluorination of carbonyl compounds
UR - http://www.scopus.com/inward/record.url?scp=85102425338&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/ee156e5a-c9db-381b-8199-dd373ef60e71/
U2 - 10.1016/j.tetlet.2021.152969
DO - 10.1016/j.tetlet.2021.152969
M3 - Article
AN - SCOPUS:85102425338
VL - 69
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
M1 - 152969
ER -
ID: 75206821