Synlett, volume 2005, issue 19, pages 2953-2957
The Reaction of Alkylenecyclopropanes and Diethyl Phosphite: A Novel Method for the Preparation of Diethyl 3,4-Dihydro-2-naphthylphosphonates and 3-Butenyl Ethyl Phosphates
Publication type: Journal Article
Publication date: 2005-10-12
Organic Chemistry
Abstract
AlBN-mediated addition of alkylidenecyclopropanes to diethyl phosphite produces diethyl-3,4-dihydro-2-naphthylphosphonates in moderate yields. When the reaction was carried out without AIBN in the presence of 5% water, 3-butenyl ethyl phosphites were obtained.
Top-30
Citations by journals
1
2
3
|
|
Tetrahedron
3 publications, 11.11%
|
|
Journal of Organic Chemistry
3 publications, 11.11%
|
|
Advanced Synthesis and Catalysis
2 publications, 7.41%
|
|
Organic Letters
2 publications, 7.41%
|
|
Beilstein Journal of Organic Chemistry
1 publication, 3.7%
|
|
Chinese Chemical Letters
1 publication, 3.7%
|
|
Journal of Organometallic Chemistry
1 publication, 3.7%
|
|
Tetrahedron Letters
1 publication, 3.7%
|
|
Chemistry - An Asian Journal
1 publication, 3.7%
|
|
European Journal of Organic Chemistry
1 publication, 3.7%
|
|
ChemInform
1 publication, 3.7%
|
|
Chemical Reviews
1 publication, 3.7%
|
|
Chemical Communications
1 publication, 3.7%
|
|
Journal of the American Chemical Society
1 publication, 3.7%
|
|
Green Chemistry
1 publication, 3.7%
|
|
Organic and Biomolecular Chemistry
1 publication, 3.7%
|
|
Organic Preparations and Procedures International
1 publication, 3.7%
|
|
Russian Chemical Reviews
1 publication, 3.7%
|
|
1
2
3
|
Citations by publishers
1
2
3
4
5
6
7
|
|
Wiley
7 publications, 25.93%
|
|
American Chemical Society (ACS)
7 publications, 25.93%
|
|
Elsevier
6 publications, 22.22%
|
|
Royal Society of Chemistry (RSC)
3 publications, 11.11%
|
|
Beilstein-Institut
1 publication, 3.7%
|
|
Taylor & Francis
1 publication, 3.7%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 3.7%
|
|
1
2
3
4
5
6
7
|
- We do not take into account publications 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":[2006,2007,2008,2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","","","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[1,1,1,4,1,2,3,0,2,2,0,0,0,3,0,2,2,2,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["3.7","3.7","3.7","14.81","3.7","7.41","11.11",0,"7.41","7.41",0,0,0,"11.11",0,"7.41","7.41","7.41","3.7"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false}},"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":["Tetrahedron","Journal of Organic Chemistry","Advanced Synthesis and Catalysis","Organic Letters","Beilstein Journal of Organic Chemistry","Chinese Chemical Letters","Journal of Organometallic Chemistry","Tetrahedron Letters","Chemistry - An Asian Journal","European Journal of Organic Chemistry","ChemInform","Chemical Reviews","Chemical Communications","Journal of the American Chemical Society","Green Chemistry","Organic and Biomolecular Chemistry","Organic Preparations and Procedures International","Russian Chemical Reviews"],"ids":[3439,8697,3906,3315,21928,20341,11834,6133,10120,19472,25372,13718,9073,4813,1017,541,5076,23802],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_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\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[3,3,2,2,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[11.11,11.11,7.41,7.41,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7,3.7],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false}},"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":["Wiley","American Chemical Society (ACS)","Elsevier","Royal Society of Chemistry (RSC)","Beilstein-Institut","Taylor & Francis","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,40,17,123,6139,18,9422],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[7,7,6,3,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[25.93,25.93,22.22,11.11,3.7,3.7,3.7],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"yearsCitationsQuartiles":{"type":"bar","data":{"show":true,"labels":[2006,2007,2008,2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0,1,0,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","3.7","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,1,0,1,0,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","3.7","0","3.7","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,0,1,1,0,0,0,0,1,0,0,0,1,0,0,1,0,0],"percentage":["0","0","0","3.7","3.7","0","0","0","0","3.7","0","0","0","3.7","0","0","3.7","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,1,1,1,0,0,1,0,2,1,0,0,0,2,0,2,1,2,1],"percentage":["0","3.7","3.7","3.7","0","0","3.7","0","7.41","3.7","0","0","0","7.41","0","7.41","3.7","7.41","3.7"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,1,0,0,2,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["3.7","0","0","3.7","0","0","7.41","0","0","0","0","0","0","0","0","0","0","0","0"]}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations quartiles by SCImago per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"yearsCitationsQuartilesWs":{"type":"bar","data":{"show":true,"labels":[2006,2007,2008,2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,2,1,1,0,0,0,1,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","7.41","3.7","3.7","0","0","0","3.7","0","0","0","0","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,0,0,0,1,0,0,0,0,0,0,0,1,0,1,2,1,0],"percentage":["0","0","0","0","0","3.7","0","0","0","0","0","0","0","3.7","0","3.7","7.41","3.7","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,1,1,1,0,0,1,0,2,1,0,0,0,2,0,1,0,1,1],"percentage":["0","3.7","3.7","3.7","0","0","3.7","0","7.41","3.7","0","0","0","7.41","0","3.7","0","3.7","3.7"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,1,0,0,2,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["3.7","0","0","3.7","0","0","7.41","0","0","0","0","0","0","0","0","0","0","0","0"]}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations quartiles by WoS per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Huang X., Yu L. The Reaction of Alkylenecyclopropanes and Diethyl Phosphite: A Novel Method for the Preparation of Diethyl 3,4-Dihydro-2-naphthylphosphonates and 3-Butenyl Ethyl Phosphates // Synlett. 2005. Vol. 2005. No. 19. pp. 2953-2957.
GOST all authors (up to 50)
Copy
Huang X., Yu L. The Reaction of Alkylenecyclopropanes and Diethyl Phosphite: A Novel Method for the Preparation of Diethyl 3,4-Dihydro-2-naphthylphosphonates and 3-Butenyl Ethyl Phosphates // Synlett. 2005. Vol. 2005. No. 19. pp. 2953-2957.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1055/s-2005-918947
UR - https://doi.org/10.1055/s-2005-918947
TI - The Reaction of Alkylenecyclopropanes and Diethyl Phosphite: A Novel Method for the Preparation of Diethyl 3,4-Dihydro-2-naphthylphosphonates and 3-Butenyl Ethyl Phosphates
T2 - Synlett
AU - Huang, Xian
AU - Yu, Lei
PY - 2005
DA - 2005/10/12 00:00:00
PB - Thieme
SP - 2953-2957
IS - 19
VL - 2005
SN - 0936-5214
SN - 1437-2096
ER -
Cite this
BibTex
Copy
@article{2005_Huang,
author = {Xian Huang and Lei Yu},
title = {The Reaction of Alkylenecyclopropanes and Diethyl Phosphite: A Novel Method for the Preparation of Diethyl 3,4-Dihydro-2-naphthylphosphonates and 3-Butenyl Ethyl Phosphates},
journal = {Synlett},
year = {2005},
volume = {2005},
publisher = {Thieme},
month = {oct},
url = {https://doi.org/10.1055/s-2005-918947},
number = {19},
pages = {2953--2957},
doi = {10.1055/s-2005-918947}
}
Cite this
MLA
Copy
Huang, Xian, and Lei Yu. “The Reaction of Alkylenecyclopropanes and Diethyl Phosphite: A Novel Method for the Preparation of Diethyl 3,4-Dihydro-2-naphthylphosphonates and 3-Butenyl Ethyl Phosphates.” Synlett, vol. 2005, no. 19, Oct. 2005, pp. 2953-2957. https://doi.org/10.1055/s-2005-918947.