A Ring-Closing Enyne Metathesis Approach to Functionalized Semicyclic Dienes: The Total Synthesis of (-)-Tetrangomycin
Publication type: Journal Article
Publication date: 2014-01-09
scimago Q2
wos Q2
SJR: 0.558
CiteScore: 4.3
Impact factor: 2.7
ISSN: 1434193X, 10990690
Organic Chemistry
Physical and Theoretical Chemistry
Abstract
The angucycline natural product (–)-tetrangomycin was synthesized from diene 37 in three steps by employing a strategy based on the Diels–Alder reaction. The synthesis of 37 was achieved through the ring-closing enyne metathesis of 13.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
2
|
|
|
European Journal of Organic Chemistry
2 publications, 14.29%
|
|
|
Coordination Chemistry Reviews
1 publication, 7.14%
|
|
|
Tetrahedron Letters
1 publication, 7.14%
|
|
|
European Journal of Medicinal Chemistry
1 publication, 7.14%
|
|
|
ChemInform
1 publication, 7.14%
|
|
|
Chemistry - A European Journal
1 publication, 7.14%
|
|
|
Angewandte Chemie - International Edition
1 publication, 7.14%
|
|
|
Angewandte Chemie
1 publication, 7.14%
|
|
|
Chemical Reviews
1 publication, 7.14%
|
|
|
Environmental Science & Technology
1 publication, 7.14%
|
|
|
Molecules
1 publication, 7.14%
|
|
|
Journal of Organic Chemistry
1 publication, 7.14%
|
|
|
Chemical Science
1 publication, 7.14%
|
|
|
1
2
|
Publishers
|
1
2
3
4
5
6
|
|
|
Wiley
6 publications, 42.86%
|
|
|
Elsevier
3 publications, 21.43%
|
|
|
American Chemical Society (ACS)
3 publications, 21.43%
|
|
|
MDPI
1 publication, 7.14%
|
|
|
Royal Society of Chemistry (RSC)
1 publication, 7.14%
|
|
|
1
2
3
4
5
6
|
- 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
14
Total citations:
14
Citations from 2024:
3
(21.43%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Moodie L. W. K., Larsen D. A Ring-Closing Enyne Metathesis Approach to Functionalized Semicyclic Dienes: The Total Synthesis of (-)-Tetrangomycin // European Journal of Organic Chemistry. 2014. Vol. 2014. No. 8. pp. 1684-1694.
GOST all authors (up to 50)
Copy
Moodie L. W. K., Larsen D. A Ring-Closing Enyne Metathesis Approach to Functionalized Semicyclic Dienes: The Total Synthesis of (-)-Tetrangomycin // European Journal of Organic Chemistry. 2014. Vol. 2014. No. 8. pp. 1684-1694.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/ejoc.201301627
UR - https://doi.org/10.1002/ejoc.201301627
TI - A Ring-Closing Enyne Metathesis Approach to Functionalized Semicyclic Dienes: The Total Synthesis of (-)-Tetrangomycin
T2 - European Journal of Organic Chemistry
AU - Moodie, Lindon W K
AU - Larsen, David
PY - 2014
DA - 2014/01/09
PB - Wiley
SP - 1684-1694
IS - 8
VL - 2014
SN - 1434-193X
SN - 1099-0690
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2014_Moodie,
author = {Lindon W K Moodie and David Larsen},
title = {A Ring-Closing Enyne Metathesis Approach to Functionalized Semicyclic Dienes: The Total Synthesis of (-)-Tetrangomycin},
journal = {European Journal of Organic Chemistry},
year = {2014},
volume = {2014},
publisher = {Wiley},
month = {jan},
url = {https://doi.org/10.1002/ejoc.201301627},
number = {8},
pages = {1684--1694},
doi = {10.1002/ejoc.201301627}
}
Cite this
MLA
Copy
Moodie, Lindon W. K., and David Larsen. “A Ring-Closing Enyne Metathesis Approach to Functionalized Semicyclic Dienes: The Total Synthesis of (-)-Tetrangomycin.” European Journal of Organic Chemistry, vol. 2014, no. 8, Jan. 2014, pp. 1684-1694. https://doi.org/10.1002/ejoc.201301627.