Rh(II)-catalysed reactions of 2H-azirines with ethyl 2-acyl-2- diazoacetates. Synthesis of novel photochromic oxazines
Publication type: Journal Article
Publication date: 2009-11-01
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
Abstract Photochromic non-fused 2 H -1,4-oxazines are synthesised by a Rh 2 (OAc) 4 -catalysed reaction of 2 Н -azirines with ethyl 2-acyl-2-diazoacetates. The reaction proceeds via the formation of an azirinium ylide which undergoes ring-opening to a 2-azadiene followed by 1,6-electrocyclisation.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
2
3
4
|
|
|
Tetrahedron
4 publications, 13.33%
|
|
|
Organic and Biomolecular Chemistry
4 publications, 13.33%
|
|
|
Journal of Organic Chemistry
4 publications, 13.33%
|
|
|
Organic Letters
2 publications, 6.67%
|
|
|
Tetrahedron Letters
1 publication, 3.33%
|
|
|
Russian Journal of General Chemistry
1 publication, 3.33%
|
|
|
Organics
1 publication, 3.33%
|
|
|
Trends in Chemistry
1 publication, 3.33%
|
|
|
Advanced Synthesis and Catalysis
1 publication, 3.33%
|
|
|
Angewandte Chemie - International Edition
1 publication, 3.33%
|
|
|
Angewandte Chemie
1 publication, 3.33%
|
|
|
ChemInform
1 publication, 3.33%
|
|
|
Chemical Reviews
1 publication, 3.33%
|
|
|
Chemical Society Reviews
1 publication, 3.33%
|
|
|
RSC Advances
1 publication, 3.33%
|
|
|
Chemical Science
1 publication, 3.33%
|
|
|
Russian Journal of Organic Chemistry
1 publication, 3.33%
|
|
|
Progress in Heterocyclic Chemistry
1 publication, 3.33%
|
|
|
1
2
3
4
|
Publishers
|
1
2
3
4
5
6
7
8
|
|
|
Elsevier
8 publications, 26.67%
|
|
|
Royal Society of Chemistry (RSC)
7 publications, 23.33%
|
|
|
American Chemical Society (ACS)
7 publications, 23.33%
|
|
|
Wiley
4 publications, 13.33%
|
|
|
Pleiades Publishing
2 publications, 6.67%
|
|
|
MDPI
1 publication, 3.33%
|
|
|
1
2
3
4
5
6
7
8
|
- 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
30
Total citations:
30
Citations from 2024:
0
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Khlebnikov V. A. et al. Rh(II)-catalysed reactions of 2H-azirines with ethyl 2-acyl-2- diazoacetates. Synthesis of novel photochromic oxazines // Tetrahedron Letters. 2009. Vol. 50. No. 47. pp. 6509-6511.
GOST all authors (up to 50)
Copy
Khlebnikov V. A., Rostovskii N. V., Novikov M. S., Khlebnikov A. F. Rh(II)-catalysed reactions of 2H-azirines with ethyl 2-acyl-2- diazoacetates. Synthesis of novel photochromic oxazines // Tetrahedron Letters. 2009. Vol. 50. No. 47. pp. 6509-6511.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.tetlet.2009.09.033
UR - https://doi.org/10.1016/j.tetlet.2009.09.033
TI - Rh(II)-catalysed reactions of 2H-azirines with ethyl 2-acyl-2- diazoacetates. Synthesis of novel photochromic oxazines
T2 - Tetrahedron Letters
AU - Khlebnikov, Vsevolod A
AU - Rostovskii, Nikolai V
AU - Novikov, Mikhail S.
AU - Khlebnikov, Alexander F
PY - 2009
DA - 2009/11/01
PB - Elsevier
SP - 6509-6511
IS - 47
VL - 50
SN - 0040-4039
SN - 1873-3581
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2009_Khlebnikov,
author = {Vsevolod A Khlebnikov and Nikolai V Rostovskii and Mikhail S. Novikov and Alexander F Khlebnikov},
title = {Rh(II)-catalysed reactions of 2H-azirines with ethyl 2-acyl-2- diazoacetates. Synthesis of novel photochromic oxazines},
journal = {Tetrahedron Letters},
year = {2009},
volume = {50},
publisher = {Elsevier},
month = {nov},
url = {https://doi.org/10.1016/j.tetlet.2009.09.033},
number = {47},
pages = {6509--6511},
doi = {10.1016/j.tetlet.2009.09.033}
}
Cite this
MLA
Copy
Khlebnikov, Vsevolod A., et al. “Rh(II)-catalysed reactions of 2H-azirines with ethyl 2-acyl-2- diazoacetates. Synthesis of novel photochromic oxazines.” Tetrahedron Letters, vol. 50, no. 47, Nov. 2009, pp. 6509-6511. https://doi.org/10.1016/j.tetlet.2009.09.033.