том 38 издание 16 страницы 2795-2798

A new synthesis of 8-methylpsoralen utilizing a palladium-copper catalyzed reaction to generate the furan ring and thus allowing for the generation of novel analogs in the 5′-position

Тип публикацииJournal Article
Дата публикации1997-04-01
SCImago Q3
WOS Q3
БС2
SJR0.285
CiteScore3.2
Impact factor1.5
ISSN00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Краткое описание
A rapid synthesis of 8-methylpsoralen is reported that utilizes a palladium-copper catalyzed reaction to generate the furan ring. Since 8-methylpsoralen is considered one of the most photodynamic methylpsoralens known and given the fact that psoralens in general have been shown to have medicinal value against bacteria and viruses, this synthesis allows for the availability to generate new derivatives by supplying a handle in the 5′-position. 1 A new synthesis of 8-methylpsoralen that allows for the modification of the 5′-position in the psoralen ring system.
Для доступа к списку цитирований публикации необходимо авторизоваться.

Топ-30

Журналы

1
2
Advanced Synthesis and Catalysis
2 публикации, 13.33%
European Journal of Organic Chemistry
2 публикации, 13.33%
Synlett
2 публикации, 13.33%
Coordination Chemistry Reviews
1 публикация, 6.67%
SN Applied Sciences
1 публикация, 6.67%
Journal of Medicinal Chemistry
1 публикация, 6.67%
Journal of Organic Chemistry
1 публикация, 6.67%
ACS Catalysis
1 публикация, 6.67%
Synthetic Communications
1 публикация, 6.67%
1
2

Издатели

1
2
3
4
Wiley
4 публикации, 26.67%
American Chemical Society (ACS)
3 публикации, 20%
Georg Thieme Verlag KG
2 публикации, 13.33%
Elsevier
1 публикация, 6.67%
Springer Nature
1 публикация, 6.67%
Taylor & Francis
1 публикация, 6.67%
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.
 Войти с ORCID
Метрики
15
Поделиться
Цитировать
ГОСТ |
Цитировать
Aquila B. M. A new synthesis of 8-methylpsoralen utilizing a palladium-copper catalyzed reaction to generate the furan ring and thus allowing for the generation of novel analogs in the 5′-position // Tetrahedron Letters. 1997. Vol. 38. No. 16. pp. 2795-2798.
ГОСТ со всеми авторами (до 50) Скопировать
Aquila B. M. A new synthesis of 8-methylpsoralen utilizing a palladium-copper catalyzed reaction to generate the furan ring and thus allowing for the generation of novel analogs in the 5′-position // Tetrahedron Letters. 1997. Vol. 38. No. 16. pp. 2795-2798.
RIS |
Цитировать
TY - JOUR
DO - 10.1016/s0040-4039(97)00509-1
UR - https://doi.org/10.1016/s0040-4039(97)00509-1
TI - A new synthesis of 8-methylpsoralen utilizing a palladium-copper catalyzed reaction to generate the furan ring and thus allowing for the generation of novel analogs in the 5′-position
T2 - Tetrahedron Letters
AU - Aquila, Brian M
PY - 1997
DA - 1997/04/01
PB - Elsevier
SP - 2795-2798
IS - 16
VL - 38
SN - 0040-4039
SN - 1873-3581
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{1997_Aquila,
author = {Brian M Aquila},
title = {A new synthesis of 8-methylpsoralen utilizing a palladium-copper catalyzed reaction to generate the furan ring and thus allowing for the generation of novel analogs in the 5′-position},
journal = {Tetrahedron Letters},
year = {1997},
volume = {38},
publisher = {Elsevier},
month = {apr},
url = {https://doi.org/10.1016/s0040-4039(97)00509-1},
number = {16},
pages = {2795--2798},
doi = {10.1016/s0040-4039(97)00509-1}
}
MLA
Цитировать
Aquila, Brian M.. “A new synthesis of 8-methylpsoralen utilizing a palladium-copper catalyzed reaction to generate the furan ring and thus allowing for the generation of novel analogs in the 5′-position.” Tetrahedron Letters, vol. 38, no. 16, Apr. 1997, pp. 2795-2798. https://doi.org/10.1016/s0040-4039(97)00509-1.
Ошибка в публикации?