2026-04-17T09:40:12Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/55322021-11-02T12:05:29Zcom_10259_3593com_10259_5086com_10259_2604col_10259_3594
Feberero, Claudia
167
500
0000-0002-7105-9785
Sedano Labrador, Carlos
b9f6b192-a1cf-434d-817b-1af0e7d81ef5
500
Suarez Pantiga, Samuel
544
500
Silva López, Carlos
0ee5b0c9-6148-4e20-8d10-a4196558fb1c
500
Sanz Díez, Roberto
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500
2020-10-29T11:06:19Z
2020-10-29T11:06:19Z
2020-10
0022-3263
http://hdl.handle.net/10259/5532
10.1021/acs.joc.0c01732
1520-6904
The reactions of o-lithiated O-aryl N,N-diethylcarbamates
with different C−N multiple bond electrophiles have been
thoroughly studied. A 1,5-O → N carbamoyl shift, a new variation
of the anionic Fries-type rearrangement, takes place when nitriles,
imines, or alkylcarbodiimides are employed. In these cases, the
carbamoyl group plays a dual role as a directing group, building up
a variety of functional groups through the 1,5-O → N carbamoyl
migration. On the other hand, the use of iso(thio)cyanates and
arylcarbodiimides led to non-rearranged o-functionalized Oarylcarbamates.
This reactivity was further computationally
explored, and the governing factor could be traced back to the
relative basicity of the alternative products (migrated vs nonmigrated
substrates). This exploration also provided interesting insights about the degree of complexation of the lithium cations onto
these substrates. A new access to useful 2-hydroxybenzophenone derivatives has also been developed.
Junta de Castilla y León and FEDER (BU291P18) and Ministerio de Ciencia e Innovación and FEDER (CTQ2016-75023-C2-1-P and 2-P)
application/pdf
eng
American Chemical Society
The Journal of Organic Chemistry. 2020, V. 85, n. 19, p. 12561–12578
https://doi.org/10.1021/acs.joc.0c01732
info:eu-repo/grantAgreement/JCyL/BU291P18
info:eu-repo/grantAgreement/MICINN/CTQ2016-75023-C2-1-P
info:eu-repo/grantAgreement/MICINN/CTQ2016-75023-C2-2-P
Aromatic compounds
Organic compounds
Rearrangement
Reaction products
Genetics
Química orgánica
Chemistry, Organic
Experimental and Computational Study of the 1,5-O → N Carbamoyl Snieckus–Fries-Type Rearrangement
info:eu-repo/semantics/article
info:eu-repo/semantics/submittedVersion
info:eu-repo/semantics/openAccess
The Journal of Organic Chemistry
85
19
12561
12578
ORIGINAL
Feberero-joc_2020.pdf
Feberero-joc_2020.pdf
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1183819
https://riubu.ubu.es/bitstream/10259/5532/1/Feberero-joc_2020.pdf
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LICENSE
license.txt
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Feberero-joc_2020.pdf.jpg
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Feberero-joc_2020.pdf.txt
Feberero-joc_2020.pdf.txt
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10259/5532
oai:riubu.ubu.es:10259/5532
2021-11-02 13:05:29.652
Repositorio Institucional de la Universidad de Burgos
bubrep@ubu.es
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