Home / Publications / Nucleophilic addition of secondary nitro compounds to acetylene

Nucleophilic addition of secondary nitro compounds to acetylene

Boris Fedorovich Kukharev 1
Boris Fedorovich Kukharev
Valery Konstantinovich Stankevich 1
Valery Konstantinovich Stankevich
Galina Romanovna Klimenko 1
Galina Romanovna Klimenko
Published 2002-04-30
CommunicationVolume 12, Issue 2, 63-64
3
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Kukharev B. F., Stankevich V. K., Klimenko G. R. Nucleophilic addition of secondary nitro compounds to acetylene // Mendeleev Communications. 2002. Vol. 12. No. 2. pp. 63-64.
GOST all authors (up to 50) Copy
Kukharev B. F., Stankevich V. K., Klimenko G. R. Nucleophilic addition of secondary nitro compounds to acetylene // Mendeleev Communications. 2002. Vol. 12. No. 2. pp. 63-64.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1070/MC2002v012n02ABEH001541
UR - https://mendcomm.colab.ws/publications/10.1070/MC2002v012n02ABEH001541
TI - Nucleophilic addition of secondary nitro compounds to acetylene
T2 - Mendeleev Communications
AU - Kukharev, Boris Fedorovich
AU - Stankevich, Valery Konstantinovich
AU - Klimenko, Galina Romanovna
PY - 2002
DA - 2002/04/30
PB - Mendeleev Communications
SP - 63-64
IS - 2
VL - 12
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2002_Kukharev,
author = {Boris Fedorovich Kukharev and Valery Konstantinovich Stankevich and Galina Romanovna Klimenko},
title = {Nucleophilic addition of secondary nitro compounds to acetylene},
journal = {Mendeleev Communications},
year = {2002},
volume = {12},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2002v012n02ABEH001541},
number = {2},
pages = {63--64},
doi = {10.1070/MC2002v012n02ABEH001541}
}
MLA
Cite this
MLA Copy
Kukharev, Boris Fedorovich, et al. “Nucleophilic addition of secondary nitro compounds to acetylene.” Mendeleev Communications, vol. 12, no. 2, Apr. 2002, pp. 63-64. https://mendcomm.colab.ws/publications/10.1070/MC2002v012n02ABEH001541.

Abstract

The products of C-vinylation were prepared in 52–65% yield by the reaction of secondary nitroalkanes with acetylene in DMSO– KOH.

References

1.
10.1070/MC2002v012n02ABEH001541_bib1_1
Perecalin
Nenasyshchennye nitrosoedineniya, 1966
2.
10.1070/MC2002v012n02ABEH001541_bib1_2
Novikov
Khimiya alifaticheskikh i alitsiklicheskikh nitrosoedinenii, 1974
4.
10.1070/MC2002v012n02ABEH001541_bib2
Trofimov
Zh. Org. Khim., 1986
5.
10.1070/MC2002v012n02ABEH001541_bib3
Coombes
1979
6.
10.1070/MC2002v012n02ABEH001541_bib4_1
Winterfeld
Chemistry of Acetylenes, 1969
7.
10.1070/MC2002v012n02ABEH001541_bib4_2
Dickstein
The Chemistry of the Carbon–Carbon Triple Bond, 1978