The decarboxylative route to azomethine ylides. Mechanism of 1,3-dipole formation
Publication type: Journal Article
Publication date: 1987-01-01
SJR: —
CiteScore: —
Impact factor: —
ISSN: 00224936
Molecular Medicine
Abstract
Evidence is presented that indicates that the decarboxylative route to azomethine ylides from both primary and secondary, cyclic and acyclic, α-amino acids involves an intermediate oxazolidin-5-one which loses carbon dioxide in a 1,3-dipolar cycloreversion reaction to generate an azomethine ylide stereospecifically.
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73
Total citations:
73
Citations from 2024:
1
(1.37%)
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GOST
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Grigg R. et al. The decarboxylative route to azomethine ylides. Mechanism of 1,3-dipole formation // Journal of the Chemical Society Chemical Communications. 1987. Vol. 2. p. 49.
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Grigg R., Idle J., McMeekin P., Vipond D. The decarboxylative route to azomethine ylides. Mechanism of 1,3-dipole formation // Journal of the Chemical Society Chemical Communications. 1987. Vol. 2. p. 49.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/c39870000049
UR - https://doi.org/10.1039/c39870000049
TI - The decarboxylative route to azomethine ylides. Mechanism of 1,3-dipole formation
T2 - Journal of the Chemical Society Chemical Communications
AU - Grigg, Ronald
AU - Idle, Jonathan
AU - McMeekin, Peter
AU - Vipond, David
PY - 1987
DA - 1987/01/01
PB - Royal Society of Chemistry (RSC)
SP - 49
IS - 2
SN - 0022-4936
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{1987_Grigg,
author = {Ronald Grigg and Jonathan Idle and Peter McMeekin and David Vipond},
title = {The decarboxylative route to azomethine ylides. Mechanism of 1,3-dipole formation},
journal = {Journal of the Chemical Society Chemical Communications},
year = {1987},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c39870000049},
number = {2},
pages = {49},
doi = {10.1039/c39870000049}
}