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
Publication type: Journal Article
Publication date: 1997-04-01
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
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.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
2
|
|
|
Advanced Synthesis and Catalysis
2 publications, 13.33%
|
|
|
European Journal of Organic Chemistry
2 publications, 13.33%
|
|
|
Synlett
2 publications, 13.33%
|
|
|
Coordination Chemistry Reviews
1 publication, 6.67%
|
|
|
SN Applied Sciences
1 publication, 6.67%
|
|
|
Journal of Medicinal Chemistry
1 publication, 6.67%
|
|
|
Journal of Organic Chemistry
1 publication, 6.67%
|
|
|
ACS Catalysis
1 publication, 6.67%
|
|
|
Synthetic Communications
1 publication, 6.67%
|
|
|
1
2
|
Publishers
|
1
2
3
4
|
|
|
Wiley
4 publications, 26.67%
|
|
|
American Chemical Society (ACS)
3 publications, 20%
|
|
|
Georg Thieme Verlag KG
2 publications, 13.33%
|
|
|
Elsevier
1 publication, 6.67%
|
|
|
Springer Nature
1 publication, 6.67%
|
|
|
Taylor & Francis
1 publication, 6.67%
|
|
|
1
2
3
4
|
- We do not take into account publications without a DOI.
- Statistics recalculated weekly.
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
15
Total citations:
15
Citations from 2025:
0
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
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.
GOST all authors (up to 50)
Copy
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.
Cite this
RIS
Copy
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 -
Cite this
BibTex (up to 50 authors)
Copy
@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}
}
Cite this
MLA
Copy
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.