An unusual way of the reaction of PI3 with norbornene and norbornadiene
Publication type: Journal Article
Publication date: 1997-03-01
scimago Q3
SJR: 0.305
CiteScore: 2.8
Impact factor: —
ISSN: 10665285, 15739171
General Chemistry
Abstract
The iodination of norbornene and norbornadiene with phosphorus triiodide in the presence and in the absence of weak electrophiles (arylsulfenamides orN-chloramines) and with elemental iodine was studied. Depending on the reaction conditions, the reactions resulted in mono- or diiodides of the norbornene and norbornadiene series. All the compounds obtained were characterized by1H and13C NMR spectra.
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Beloglazkina E. K. et al. An unusual way of the reaction of PI3 with norbornene and norbornadiene // Russian Chemical Bulletin. 1997. Vol. 46. No. 3. pp. 496-500.
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Beloglazkina E. K., Tyurin V. S., Zyk N. V., Grishin Yu. K. An unusual way of the reaction of PI3 with norbornene and norbornadiene // Russian Chemical Bulletin. 1997. Vol. 46. No. 3. pp. 496-500.
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TY - JOUR
DO - 10.1007/BF02495403
UR - http://link.springer.com/10.1007/BF02495403
TI - An unusual way of the reaction of PI3 with norbornene and norbornadiene
T2 - Russian Chemical Bulletin
AU - Beloglazkina, E K
AU - Tyurin, V S
AU - Zyk, N. V.
AU - Grishin, Yu K
PY - 1997
DA - 1997/03/01
PB - Springer Nature
SP - 496-500
IS - 3
VL - 46
SN - 1066-5285
SN - 1573-9171
ER -
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BibTex (up to 50 authors)
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@article{1997_Beloglazkina,
author = {E K Beloglazkina and V S Tyurin and N. V. Zyk and Yu K Grishin},
title = {An unusual way of the reaction of PI3 with norbornene and norbornadiene},
journal = {Russian Chemical Bulletin},
year = {1997},
volume = {46},
publisher = {Springer Nature},
month = {mar},
url = {http://link.springer.com/10.1007/BF02495403},
number = {3},
pages = {496--500},
doi = {10.1007/BF02495403}
}
Cite this
MLA
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Beloglazkina, E. K., et al. āAn unusual way of the reaction of PI3 with norbornene and norbornadiene.ā Russian Chemical Bulletin, vol. 46, no. 3, Mar. 1997, pp. 496-500. http://link.springer.com/10.1007/BF02495403.
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