том 51 издание 1 страницы 17-25

Synthesis of 2-(chloro(methoxy, morpholino)methyl)-hexahydropyrimidothieno[3,2-c]azocines and tetrahydrospiro[pyrido[4,5']thieno[2,3-d]pyrimidines]

Тип публикацииJournal Article
Дата публикации2015-01-01
scimago Q4
wos Q4
БС3
SJR0.243
CiteScore2.7
Impact factor1.0
ISSN00093122, 15738353
Organic Chemistry
Краткое описание
2-(Chloromethyl)-5,6,7,8-tetrahydropyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4(3Н)-ones reacted with acetylenedicarboxylate ester, methyl propiolate or acetylacetylene, forming mixtures of 2-(chloromethyl)-5,6,7,10-tetrahydropyrimido[5',4':4,5]thieno[3,2-d]azocin-4(3Н)-ones and 2'-chloromethyl-6'-methylidene-2,3-dihydro-1Н-spiro[pyrido[4,5']thieno[2,3-d]pyrimidin]-4'(3'H)-ones in various ratios. Analogous products were also obtained in the reaction of 2-(methoxymethyl) derivative with methyl propiolate, while using 2-[(morpholin-4-yl)-methyl] derivative in a similar reaction led to the formation of a more complex product mixture.
Найдено 
Найдено 

Топ-30

Журналы

1
2
3
Chemistry of Heterocyclic Compounds
3 публикации, 33.33%
Scientific Reports
1 публикация, 11.11%
Bioorganic and Medicinal Chemistry
1 публикация, 11.11%
ChemInform
1 публикация, 11.11%
European Journal of Organic Chemistry
1 публикация, 11.11%
Synthesis
1 публикация, 11.11%
Russian Chemical Reviews
1 публикация, 11.11%
1
2
3

Издатели

1
2
3
4
Springer Nature
4 публикации, 44.44%
Wiley
2 публикации, 22.22%
Elsevier
1 публикация, 11.11%
Georg Thieme Verlag KG
1 публикация, 11.11%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 публикация, 11.11%
1
2
3
4
  • Мы не учитываем публикации, у которых нет DOI.
  • Статистика публикаций обновляется еженедельно.

Вы ученый?

Создайте профиль, чтобы получать персональные рекомендации коллег, конференций и новых статей.
Метрики
9
Поделиться
Цитировать
ГОСТ |
Цитировать
Voskressensky L. G. et al. Synthesis of 2-(chloro(methoxy, morpholino)methyl)-hexahydropyrimidothieno[3,2-c]azocines and tetrahydrospiro[pyrido[4,5']thieno[2,3-d]pyrimidines] // Chemistry of Heterocyclic Compounds. 2015. Vol. 51. No. 1. pp. 17-25.
ГОСТ со всеми авторами (до 50) Скопировать
Voskressensky L. G., Kovaleva S. A., Borisova T. N., Titov A. A., Toze F., Listratova A. V., Khrustalev V. N., Varlamov A. V. Synthesis of 2-(chloro(methoxy, morpholino)methyl)-hexahydropyrimidothieno[3,2-c]azocines and tetrahydrospiro[pyrido[4,5']thieno[2,3-d]pyrimidines] // Chemistry of Heterocyclic Compounds. 2015. Vol. 51. No. 1. pp. 17-25.
RIS |
Цитировать
TY - JOUR
DO - 10.1007/s10593-015-1652-2
UR - https://doi.org/10.1007/s10593-015-1652-2
TI - Synthesis of 2-(chloro(methoxy, morpholino)methyl)-hexahydropyrimidothieno[3,2-c]azocines and tetrahydrospiro[pyrido[4,5']thieno[2,3-d]pyrimidines]
T2 - Chemistry of Heterocyclic Compounds
AU - Voskressensky, Leonid G
AU - Kovaleva, Svetlana A
AU - Borisova, Tatiana N
AU - Titov, Alexander A
AU - Toze, Flavien
AU - Listratova, Anna V.
AU - Khrustalev, Viktor N
AU - Varlamov, Alexey V
PY - 2015
DA - 2015/01/01
PB - Springer Nature
SP - 17-25
IS - 1
VL - 51
SN - 0009-3122
SN - 1573-8353
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2015_Voskressensky,
author = {Leonid G Voskressensky and Svetlana A Kovaleva and Tatiana N Borisova and Alexander A Titov and Flavien Toze and Anna V. Listratova and Viktor N Khrustalev and Alexey V Varlamov},
title = {Synthesis of 2-(chloro(methoxy, morpholino)methyl)-hexahydropyrimidothieno[3,2-c]azocines and tetrahydrospiro[pyrido[4,5']thieno[2,3-d]pyrimidines]},
journal = {Chemistry of Heterocyclic Compounds},
year = {2015},
volume = {51},
publisher = {Springer Nature},
month = {jan},
url = {https://doi.org/10.1007/s10593-015-1652-2},
number = {1},
pages = {17--25},
doi = {10.1007/s10593-015-1652-2}
}
MLA
Цитировать
Voskressensky, Leonid G., et al. “Synthesis of 2-(chloro(methoxy, morpholino)methyl)-hexahydropyrimidothieno[3,2-c]azocines and tetrahydrospiro[pyrido[4,5']thieno[2,3-d]pyrimidines].” Chemistry of Heterocyclic Compounds, vol. 51, no. 1, Jan. 2015, pp. 17-25. https://doi.org/10.1007/s10593-015-1652-2.