том 56 издание 4 страницы 569-575

Heptalene Synthesis by Addition of Aryl Acetylenes to Azulenes

Тип публикацииJournal Article
Дата публикации2020-04-01
SCImago Q4
WOS Q4
БС3
SJR0.187
CiteScore1.3
Impact factor0.9
ISSN10704280, 16083393
Organic Chemistry
Краткое описание
Abstract Aryl acetylenes bearing electron-withdrawing groups have been found that can add to azulenes and yield 1,2-substituted heptalenes. Theoretical studies of the reaction mechanism helped to design the candidate molecules that have then been tested in the synthetic work. New heptalenes are obtained by reacting methyl (4-nitrophenyl)propiolate with either 4,6,8-trimethylazulene or guaiazulene, as well as 3-(4-nitrophenyl)-2-propyn-1-ol with guaiazulene. This opens a new synthetic route to 1-aryl-substituted heptalenes.
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ГОСТ |
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Briling K. R. et al. Heptalene Synthesis by Addition of Aryl Acetylenes to Azulenes // Russian Journal of Organic Chemistry. 2020. Vol. 56. No. 4. pp. 569-575.
ГОСТ со всеми авторами (до 50) Скопировать
Briling K. R., Laikov D. Heptalene Synthesis by Addition of Aryl Acetylenes to Azulenes // Russian Journal of Organic Chemistry. 2020. Vol. 56. No. 4. pp. 569-575.
RIS |
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TY - JOUR
DO - 10.1134/S1070428020040028
UR - https://link.springer.com/10.1134/S1070428020040028
TI - Heptalene Synthesis by Addition of Aryl Acetylenes to Azulenes
T2 - Russian Journal of Organic Chemistry
AU - Briling, K R
AU - Laikov, D.N.
PY - 2020
DA - 2020/04/01
PB - Pleiades Publishing
SP - 569-575
IS - 4
VL - 56
SN - 1070-4280
SN - 1608-3393
ER -
BibTex |
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@article{2020_Briling,
author = {K R Briling and D.N. Laikov},
title = {Heptalene Synthesis by Addition of Aryl Acetylenes to Azulenes},
journal = {Russian Journal of Organic Chemistry},
year = {2020},
volume = {56},
publisher = {Pleiades Publishing},
month = {apr},
url = {https://link.springer.com/10.1134/S1070428020040028},
number = {4},
pages = {569--575},
doi = {10.1134/S1070428020040028}
}
MLA
Цитировать
Briling, K. R., et al. “Heptalene Synthesis by Addition of Aryl Acetylenes to Azulenes.” Russian Journal of Organic Chemistry, vol. 56, no. 4, Apr. 2020, pp. 569-575. https://link.springer.com/10.1134/S1070428020040028.
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