Research output: Contribution to journal › Article › peer-review
Reaction of 3,3,3-Tribromo- and 1,3,3,3-Tetrabromo-1-nitroprop-1-enes with Aliphatic Dienes. / Anisimova, N. A.; Slobodchikova, E. K.; Ivanova, M. E. et al.
In: Russian Journal of General Chemistry, Vol. 90, No. 8, 01.08.2020, p. 1388-1397.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Reaction of 3,3,3-Tribromo- and 1,3,3,3-Tetrabromo-1-nitroprop-1-enes with Aliphatic Dienes
AU - Anisimova, N. A.
AU - Slobodchikova, E. K.
AU - Ivanova, M. E.
AU - Rybalova, T. V.
PY - 2020/8/1
Y1 - 2020/8/1
N2 - 3,3,3-Tribromo- and 1,3,3,3-tetrabromo-1-nitroprop-1-enes reacted with2-methyl- and 2,3-dimethylbuta-1,3-dienes to give cyclohexene, cyclohexane, andhepta-1,5-diene derivatives containing nitro and tribromomethyl groups. Theproducts were characterized by IR and 1H and13C NMR spectra and X-ray diffractiondata.
AB - 3,3,3-Tribromo- and 1,3,3,3-tetrabromo-1-nitroprop-1-enes reacted with2-methyl- and 2,3-dimethylbuta-1,3-dienes to give cyclohexene, cyclohexane, andhepta-1,5-diene derivatives containing nitro and tribromomethyl groups. Theproducts were characterized by IR and 1H and13C NMR spectra and X-ray diffractiondata.
KW - 1,4-addition
KW - 3,3,3-tribromo-1-nitroprop-1-ene
KW - cyclohexene derivatives
KW - Diels–Alder reaction
KW - hepta-1,5-diene
UR - http://www.scopus.com/inward/record.url?scp=85091121712&partnerID=8YFLogxK
U2 - 10.1134/S1070363220080022
DO - 10.1134/S1070363220080022
M3 - Article
AN - SCOPUS:85091121712
VL - 90
SP - 1388
EP - 1397
JO - Russian Journal of General Chemistry
JF - Russian Journal of General Chemistry
SN - 1070-3632
IS - 8
ER -
ID: 25651205