Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective

Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective Review

Journal

Beilstein Journal of Organic Chemistry
ISSN: 2195-951X , E-ISSN: 1860-5397

Output data

Year: 2017, Volume: 13, Pages: 2214-2234 Pages count : 21 DOI: 10.3762/bjoc.13.220

Authors

Boyko Yaroslav Dmitrievich ^1,2 , Dorokhov Valentin Sergeevich ^1,2 , Sukhorukov Alexey Yu ^1,2 , Ioffe Sema Leibovich ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, 119991, Leninsky prospect, 47, Moscow, Russia.
2	Higher Chemical College, D. Mendeleev University of Chemical Technology of Russia, 125047, Miusskaya sq., 9, Moscow, Russia

Despite of their chemical instability and high reactivity, conjugated nitrosoalkenes are useful intermediates in target-oriented organic synthesis. The present review deals with carbon–carbon bond forming reactions involving Michael addition to α-nitrosoalkenes with a particular focus on recent developments in this methodology and its use in total synthesis.

Boyko Y.D. , Dorokhov V.S. , Sukhorukov A.Y. , Ioffe S.L.
Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective
Beilstein Journal of Organic Chemistry. 2017. V.13. P.2214-2234. DOI: 10.3762/bjoc.13.220 WOS Scopus OpenAlex

Web of science:	WOS:000413583200001
Scopus:	2-s2.0-85033591174
OpenAlex:	W2766373320

DB	Citing
OpenAlex	27
Scopus	27
Web of science	27