Tetrahedron Letters, volume 54, issue 27, pages 3507-3509
Synthesis of monocyclic nine-membered compounds by the [4+3+2] cycloaddition-bond cleavage strategy
Publication type: Journal Article
Publication date: 2013-07-01
Journal:
Tetrahedron Letters
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.8
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
Monocyclic nine-membered compounds were synthesized by the cleavage of the six-membered ring of the bicyclic compounds. Thus, the bicyclic compounds which consist of six- and nine-membered rings were synthesized by the Ni-catalyzed [4+3+2] cycloaddition, and the cleavage of the N–O bond, which was incorporated in the six-membered ring, proceeded in the presence of Mo(CO)6 to yield the monocyclic compound. On the other hand, the cleavage of the C–O bond proceeded efficiently in the presence of SmI2.
Top-30
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Organic and Biomolecular Chemistry
3 publications, 20%
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Organic Letters
2 publications, 13.33%
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Angewandte Chemie - International Edition
1 publication, 6.67%
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1 publication, 6.67%
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1 publication, 6.67%
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1 publication, 6.67%
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1 publication, 6.67%
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1 publication, 6.67%
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Russian Chemical Reviews
1 publication, 6.67%
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1
2
3
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Citations by publishers
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6
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Wiley
6 publications, 40%
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Royal Society of Chemistry (RSC)
4 publications, 26.67%
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American Chemical Society (ACS)
3 publications, 20%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 6.67%
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- 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.
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Yamasaki R. et al. Synthesis of monocyclic nine-membered compounds by the [4+3+2] cycloaddition-bond cleavage strategy // Tetrahedron Letters. 2013. Vol. 54. No. 27. pp. 3507-3509.
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Yamasaki R., Kato K., Hanitani D., Mutoh Y., SAITO S. Synthesis of monocyclic nine-membered compounds by the [4+3+2] cycloaddition-bond cleavage strategy // Tetrahedron Letters. 2013. Vol. 54. No. 27. pp. 3507-3509.
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TY - JOUR
DO - 10.1016/j.tetlet.2013.04.094
UR - https://doi.org/10.1016/j.tetlet.2013.04.094
TI - Synthesis of monocyclic nine-membered compounds by the [4+3+2] cycloaddition-bond cleavage strategy
T2 - Tetrahedron Letters
AU - Yamasaki, Ryu
AU - Kato, Korehito
AU - Hanitani, Daichi
AU - Mutoh, Yuichiro
AU - SAITO, Shinichi
PY - 2013
DA - 2013/07/01 00:00:00
PB - Elsevier
SP - 3507-3509
IS - 27
VL - 54
SN - 0040-4039
SN - 1873-3581
ER -
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@article{2013_Yamasaki,
author = {Ryu Yamasaki and Korehito Kato and Daichi Hanitani and Yuichiro Mutoh and Shinichi SAITO},
title = {Synthesis of monocyclic nine-membered compounds by the [4+3+2] cycloaddition-bond cleavage strategy},
journal = {Tetrahedron Letters},
year = {2013},
volume = {54},
publisher = {Elsevier},
month = {jul},
url = {https://doi.org/10.1016/j.tetlet.2013.04.094},
number = {27},
pages = {3507--3509},
doi = {10.1016/j.tetlet.2013.04.094}
}
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Yamasaki, Ryu, et al. “Synthesis of monocyclic nine-membered compounds by the [4+3+2] cycloaddition-bond cleavage strategy.” Tetrahedron Letters, vol. 54, no. 27, Jul. 2013, pp. 3507-3509. https://doi.org/10.1016/j.tetlet.2013.04.094.