Metal promoted higher-order cycloaddition reactions. A facile entry into substituted eight- and ten-membered carbocycles.
Publication type: Journal Article
Publication date: 1992-09-01
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
Substituted eight- and ten-membered carbocycles can be accessed by employing a metal promoted higher-order cycloaddition of heterocyclic trienes followed by heteroatom extrusion.
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43
Total citations:
43
Citations from 2025:
1
(2.33%)
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MLA
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GOST
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Rigby J. H., Ateeq H. S., Krueger A. Metal promoted higher-order cycloaddition reactions. A facile entry into substituted eight- and ten-membered carbocycles. // Tetrahedron Letters. 1992. Vol. 33. No. 40. pp. 5873-5876.
GOST all authors (up to 50)
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Rigby J. H., Ateeq H. S., Krueger A. Metal promoted higher-order cycloaddition reactions. A facile entry into substituted eight- and ten-membered carbocycles. // Tetrahedron Letters. 1992. Vol. 33. No. 40. pp. 5873-5876.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/S0040-4039(00)61076-6
UR - https://doi.org/10.1016/S0040-4039(00)61076-6
TI - Metal promoted higher-order cycloaddition reactions. A facile entry into substituted eight- and ten-membered carbocycles.
T2 - Tetrahedron Letters
AU - Rigby, James H.
AU - Ateeq, Humy S
AU - Krueger, A.Chris
PY - 1992
DA - 1992/09/01
PB - Elsevier
SP - 5873-5876
IS - 40
VL - 33
SN - 0040-4039
SN - 1873-3581
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{1992_Rigby,
author = {James H. Rigby and Humy S Ateeq and A.Chris Krueger},
title = {Metal promoted higher-order cycloaddition reactions. A facile entry into substituted eight- and ten-membered carbocycles.},
journal = {Tetrahedron Letters},
year = {1992},
volume = {33},
publisher = {Elsevier},
month = {sep},
url = {https://doi.org/10.1016/S0040-4039(00)61076-6},
number = {40},
pages = {5873--5876},
doi = {10.1016/S0040-4039(00)61076-6}
}
Cite this
MLA
Copy
Rigby, James H., et al. “Metal promoted higher-order cycloaddition reactions. A facile entry into substituted eight- and ten-membered carbocycles..” Tetrahedron Letters, vol. 33, no. 40, Sep. 1992, pp. 5873-5876. https://doi.org/10.1016/S0040-4039(00)61076-6.