Asymmetric amination of carboxylic acids via a diels-alder strategy.
Publication type: Journal Article
Publication date: 1991-09-01
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
2-azadienes 1 which are readily prepared from acyl chlorides react with high facial selectivity with the chiral carbamoyl nitroso dicnophile 2. Reduction and hydrolysis of the adducts yield enantiomerically pure amino acids.
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Total citations:
44
Citations from 2024:
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GOST
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Gouverneur V., Ghosez L. Asymmetric amination of carboxylic acids via a diels-alder strategy. // Tetrahedron Letters. 1991. Vol. 32. No. 39. pp. 5349-5352.
GOST all authors (up to 50)
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Gouverneur V., Ghosez L. Asymmetric amination of carboxylic acids via a diels-alder strategy. // Tetrahedron Letters. 1991. Vol. 32. No. 39. pp. 5349-5352.
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RIS
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TY - JOUR
DO - 10.1016/s0040-4039(00)92382-7
UR - https://doi.org/10.1016/s0040-4039(00)92382-7
TI - Asymmetric amination of carboxylic acids via a diels-alder strategy.
T2 - Tetrahedron Letters
AU - Gouverneur, Véronique
AU - Ghosez, L.
PY - 1991
DA - 1991/09/01
PB - Elsevier
SP - 5349-5352
IS - 39
VL - 32
SN - 0040-4039
SN - 1873-3581
ER -
Cite this
BibTex (up to 50 authors)
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@article{1991_Gouverneur,
author = {Véronique Gouverneur and L. Ghosez},
title = {Asymmetric amination of carboxylic acids via a diels-alder strategy.},
journal = {Tetrahedron Letters},
year = {1991},
volume = {32},
publisher = {Elsevier},
month = {sep},
url = {https://doi.org/10.1016/s0040-4039(00)92382-7},
number = {39},
pages = {5349--5352},
doi = {10.1016/s0040-4039(00)92382-7}
}
Cite this
MLA
Copy
Gouverneur, Véronique, and L. Ghosez. “Asymmetric amination of carboxylic acids via a diels-alder strategy..” Tetrahedron Letters, vol. 32, no. 39, Sep. 1991, pp. 5349-5352. https://doi.org/10.1016/s0040-4039(00)92382-7.