Tetrahedron Letters, volume 51, issue 50, pages 6498-6499
A new method for the synthesis of the marine alkaloid fascaplysin
Publication type: Journal Article
Publication date: 2010-12-01
Journal:
Tetrahedron Letters
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.8
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
A new method for the synthesis of the marine alkaloid fascaplysin has been developed via a simple and practical approach to pyrido[1,2- a :3,4- b ′]diindole ring system formation. Conversion of the marine alkaloid homofascaplysin C into fascaplysin is also described.
Citations by journals
1
2
3
4
5
|
|
Marine Drugs
|
Marine Drugs
5 publications, 18.52%
|
Tetrahedron Letters
|
Tetrahedron Letters
4 publications, 14.81%
|
Organic Letters
|
Organic Letters
2 publications, 7.41%
|
RSC Advances
|
RSC Advances
2 publications, 7.41%
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
1 publication, 3.7%
|
Journal of Pharmaceutical and Biomedical Analysis
|
Journal of Pharmaceutical and Biomedical Analysis
1 publication, 3.7%
|
Tetrahedron
|
Tetrahedron
1 publication, 3.7%
|
Advanced Synthesis and Catalysis
|
Advanced Synthesis and Catalysis
1 publication, 3.7%
|
European Journal of Organic Chemistry
|
European Journal of Organic Chemistry
1 publication, 3.7%
|
Chemical Reviews
|
Chemical Reviews
1 publication, 3.7%
|
ACS Omega
|
ACS Omega
1 publication, 3.7%
|
MedChemComm
|
MedChemComm
1 publication, 3.7%
|
Natural Product Reports
|
Natural Product Reports
1 publication, 3.7%
|
Organic Chemistry Frontiers
|
Organic Chemistry Frontiers
1 publication, 3.7%
|
Organic and Biomolecular Chemistry
|
Organic and Biomolecular Chemistry
1 publication, 3.7%
|
Synlett
|
Synlett
1 publication, 3.7%
|
1
2
3
4
5
|
Citations by publishers
1
2
3
4
5
6
|
|
Elsevier
|
Elsevier
6 publications, 22.22%
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
6 publications, 22.22%
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
5 publications, 18.52%
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
4 publications, 14.81%
|
Wiley
|
Wiley
2 publications, 7.41%
|
Springer Nature
|
Springer Nature
1 publication, 3.7%
|
Thieme
|
Thieme
1 publication, 3.7%
|
1
2
3
4
5
6
|
- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
{"yearsCitations":{"type":"bar","data":{"show":true,"labels":[2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[1,1,6,3,0,2,1,4,3,0,2,1,2,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["3.7","3.7","22.22","11.11",0,"7.41","3.7","14.81","11.11",0,"7.41","3.7","7.41","3.7"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"journals":{"type":"bar","data":{"show":true,"labels":["Marine Drugs","Tetrahedron Letters","Organic Letters","RSC Advances","Chemistry of Heterocyclic Compounds","Journal of Pharmaceutical and Biomedical Analysis","Tetrahedron","Advanced Synthesis and Catalysis","European Journal of Organic Chemistry","Chemical Reviews","ACS Omega","MedChemComm","Natural Product Reports","Organic Chemistry Frontiers","Organic and Biomolecular Chemistry","Synlett"],"ids":[23709,6133,3315,3100,16828,23304,3439,3906,19472,13718,18901,23868,15252,3991,541,10217],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp"],"datasets":[{"label":"","data":[5,4,2,2,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[18.52,14.81,7.41,7.41,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Journals","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"publishers":{"type":"bar","data":{"show":true,"labels":["Elsevier","Royal Society of Chemistry (RSC)","Multidisciplinary Digital Publishing Institute (MDPI)","American Chemical Society (ACS)","Wiley","Springer Nature","Thieme"],"ids":[17,123,202,40,11,8,135],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp"],"datasets":[{"label":"","data":[6,6,5,4,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[22.22,22.22,18.52,14.81,7.41,3.7,3.7],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Zhidkov M. E. et al. A new method for the synthesis of the marine alkaloid fascaplysin // Tetrahedron Letters. 2010. Vol. 51. No. 50. pp. 6498-6499.
GOST all authors (up to 50)
Copy
Zhidkov M. E., Baranova O. V., Kravchenko N. S., Dubovitskii S. V. A new method for the synthesis of the marine alkaloid fascaplysin // Tetrahedron Letters. 2010. Vol. 51. No. 50. pp. 6498-6499.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.tetlet.2010.09.120
UR - https://doi.org/10.1016%2Fj.tetlet.2010.09.120
TI - A new method for the synthesis of the marine alkaloid fascaplysin
T2 - Tetrahedron Letters
AU - Zhidkov, Maxim E
AU - Baranova, Olga V.
AU - Kravchenko, Natalya S
AU - Dubovitskii, Sergey V.
PY - 2010
DA - 2010/12/01 00:00:00
PB - Elsevier
SP - 6498-6499
IS - 50
VL - 51
SN - 0040-4039
SN - 1873-3581
ER -
Cite this
BibTex
Copy
@article{2010_Zhidkov,
author = {Maxim E Zhidkov and Olga V. Baranova and Natalya S Kravchenko and Sergey V. Dubovitskii},
title = {A new method for the synthesis of the marine alkaloid fascaplysin},
journal = {Tetrahedron Letters},
year = {2010},
volume = {51},
publisher = {Elsevier},
month = {dec},
url = {https://doi.org/10.1016%2Fj.tetlet.2010.09.120},
number = {50},
pages = {6498--6499},
doi = {10.1016/j.tetlet.2010.09.120}
}
Cite this
MLA
Copy
Zhidkov, Maxim E., et al. “A new method for the synthesis of the marine alkaloid fascaplysin.” Tetrahedron Letters, vol. 51, no. 50, Dec. 2010, pp. 6498-6499. https://doi.org/10.1016%2Fj.tetlet.2010.09.120.
Profiles