Organic Letters, volume 8, issue 20, pages 4529-4532
Synthesis of 1,4-dithiins from pentathiepins
Publication type: Journal Article
Publication date: 2006-09-01
Journal:
Organic Letters
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.2
ISSN: 15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
Fused aromatic and heterocyclic 1,2,3,4,5-pentathiepins react with triphenylphosphine and alkynes bearing electron-withdrawing groups to give the corresponding 1,4-dithiins in high yields. Unsymmetrical alkynes add regioselectively to afford products in agreement with the electron distribution in a proposed reaction intermediate. A mechanism for these reactions is proposed.
Citations by journals
1
2
3
|
|
Progress in Heterocyclic Chemistry
|
Progress in Heterocyclic Chemistry
3 publications, 15.79%
|
Tetrahedron
|
Tetrahedron
1 publication, 5.26%
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
1 publication, 5.26%
|
Mendeleev Communications
|
Mendeleev Communications
1 publication, 5.26%
|
Current Organic Chemistry
|
Current Organic Chemistry
1 publication, 5.26%
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
1 publication, 5.26%
|
Synthesis
|
Synthesis
1 publication, 5.26%
|
ChemInform
|
ChemInform
1 publication, 5.26%
|
Journal of Heterocyclic Chemistry
|
Journal of Heterocyclic Chemistry
1 publication, 5.26%
|
Chemical Communications
|
Chemical Communications
1 publication, 5.26%
|
Russian Journal of Organic Chemistry
|
Russian Journal of Organic Chemistry
1 publication, 5.26%
|
Journal of Sulfur Chemistry
|
Journal of Sulfur Chemistry
1 publication, 5.26%
|
Heterocycles
|
Heterocycles
1 publication, 5.26%
|
Organic Chemistry Frontiers
|
Organic Chemistry Frontiers
1 publication, 5.26%
|
Synlett
|
Synlett
1 publication, 5.26%
|
1
2
3
|
Citations by publishers
1
2
3
4
5
|
|
Elsevier
|
Elsevier
5 publications, 26.32%
|
Thieme
|
Thieme
2 publications, 10.53%
|
Wiley
|
Wiley
2 publications, 10.53%
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
2 publications, 10.53%
|
Springer Nature
|
Springer Nature
1 publication, 5.26%
|
Bentham Science
|
Bentham Science
1 publication, 5.26%
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
1 publication, 5.26%
|
Pleiades Publishing
|
Pleiades Publishing
1 publication, 5.26%
|
Taylor & Francis
|
Taylor & Francis
1 publication, 5.26%
|
The Japan Institute of Heterocyclic Chemistry
|
The Japan Institute of Heterocyclic Chemistry
1 publication, 5.26%
|
1
2
3
4
5
|
- 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":[2006,2007,2008,2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023],"ids":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[1,2,5,3,0,0,3,0,0,1,0,0,1,0,0,0,1,2],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["5.26","10.53","26.32","15.79",0,0,"15.79",0,0,"5.26",0,0,"5.26",0,0,0,"5.26","10.53"],"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":["Progress in Heterocyclic Chemistry","Tetrahedron","Russian Chemical Bulletin","Mendeleev Communications","Current Organic Chemistry","Journal of Organic Chemistry","Synthesis","ChemInform","Journal of Heterocyclic Chemistry","Chemical Communications","Russian Journal of Organic Chemistry","Journal of Sulfur Chemistry","Heterocycles","Organic Chemistry Frontiers","Synlett"],"ids":[17224,3439,10918,5294,16175,8697,10934,25372,3189,9073,5728,536,22287,3991,10217],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/doUaFUZdxUEQjLi1TwZjGHi8HXYNWWSk04dSC6Xh_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/SovkqI6gX6to8o5XBnS9RNxEOYVicn7hatkMzrvl_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp"],"datasets":[{"label":"","data":[3,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[15.79,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26,5.26],"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","Thieme","Wiley","Royal Society of Chemistry (RSC)","Springer Nature","Bentham Science","American Chemical Society (ACS)","Pleiades Publishing","Taylor & Francis","The Japan Institute of Heterocyclic Chemistry"],"ids":[17,135,11,123,8,39,40,101,18,9411],"codes":[0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/doUaFUZdxUEQjLi1TwZjGHi8HXYNWWSk04dSC6Xh_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/SovkqI6gX6to8o5XBnS9RNxEOYVicn7hatkMzrvl_medium.webp"],"datasets":[{"label":"","data":[5,2,2,2,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[26.32,10.53,10.53,10.53,5.26,5.26,5.26,5.26,5.26,5.26],"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
Amelichev S. A. et al. Synthesis of 1,4-dithiins from pentathiepins // Organic Letters. 2006. Vol. 8. No. 20. pp. 4529-4532.
GOST all authors (up to 50)
Copy
Amelichev S. A., Konstantinova L. S., Obruchnikova N. V., Rakitin O. A., Rees C. W. Synthesis of 1,4-dithiins from pentathiepins // Organic Letters. 2006. Vol. 8. No. 20. pp. 4529-4532.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/ol0617042
UR - https://doi.org/10.1021%2Fol0617042
TI - Synthesis of 1,4-dithiins from pentathiepins
T2 - Organic Letters
AU - Amelichev, Stanislav A.
AU - Konstantinova, Lidia S.
AU - Obruchnikova, Natalia V.
AU - Rees, Charles W.
AU - Rakitin, Oleg A.
PY - 2006
DA - 2006/09/01 00:00:00
PB - American Chemical Society (ACS)
SP - 4529-4532
IS - 20
VL - 8
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex
Copy
@article{2006_Amelichev,
author = {Stanislav A. Amelichev and Lidia S. Konstantinova and Natalia V. Obruchnikova and Charles W. Rees and Oleg A. Rakitin},
title = {Synthesis of 1,4-dithiins from pentathiepins},
journal = {Organic Letters},
year = {2006},
volume = {8},
publisher = {American Chemical Society (ACS)},
month = {sep},
url = {https://doi.org/10.1021%2Fol0617042},
number = {20},
pages = {4529--4532},
doi = {10.1021/ol0617042}
}
Cite this
MLA
Copy
Amelichev, Stanislav A., et al. “Synthesis of 1,4-dithiins from pentathiepins.” Organic Letters, vol. 8, no. 20, Sep. 2006, pp. 4529-4532. https://doi.org/10.1021%2Fol0617042.