Zobrazeno 1 - 10
of 149
pro vyhledávání: '"Hélène Lebel"'
Publikováno v:
Journal of Flow Chemistry. 13:21-29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e8e5cfcff431916d2a7a91dc4e0df12
https://doi.org/10.1007/s41981-022-00246-w
https://doi.org/10.1007/s41981-022-00246-w
Publikováno v:
New Journal of Chemistry. 46:21085-21091
A novel rational to account for the selectivity of 5-substituted 1H-tetrazole alkylation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4993e36eb266af5885e6aebd67c7b82
https://doi.org/10.1039/d2nj03841b
https://doi.org/10.1039/d2nj03841b
Publikováno v:
Organometallics. 40:3267-3275
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6fc9c7bb4e524cf3c88778269d550dd
https://doi.org/10.1021/acs.organomet.1c00367
https://doi.org/10.1021/acs.organomet.1c00367
Autor:
Hélène Lebel, Guillaume Reynard
Publikováno v:
The Journal of Organic Chemistry. 86:12452-12459
A new alkylation reaction of monosubstituted tetrazoles via the diazotization of aliphatic amines is reported. This method enables preferential formation of 2,5-disubstituted tetrazoles. A one-pot 1,3-dipolar cycloaddition/diazotization sequence star
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98a671275a5c2e2557f6252d9bfe65e0
https://doi.org/10.1021/acs.joc.1c01585
https://doi.org/10.1021/acs.joc.1c01585
Autor:
Hélène Lebel
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis. :1-3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5da2ca92f0a5efa6d1c75e999a3da63a
https://doi.org/10.1002/047084289x.rn02256.pub2
https://doi.org/10.1002/047084289x.rn02256.pub2
Publikováno v:
Canadian Journal of Chemistry. 98:480-484
In this paper, the synthesis of alkyl aryl ethers from electron poor phenols and amines, using 1,3-propanedinitrite, is described. Due to the mild conditions, functionalized primary, secondary, and tertiary alkyl groups were successfully introduced,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f9e3edbf26ed922cd38b4b13139f185
https://doi.org/10.1139/cjc-2020-0028
https://doi.org/10.1139/cjc-2020-0028
Publikováno v:
Organic Process Research & Development. 24:2157-2168
The first continuous flow process was developed to synthesize N-methyl secondary amines from alkyl mesylates and epoxides via a nucleophilic substitution using aqueous methylamine. A variety of N-m...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04427ac4a211689febf9531e33d3fd67
https://doi.org/10.1021/acs.oprd.0c00193
https://doi.org/10.1021/acs.oprd.0c00193
Publikováno v:
Organic Syntheses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10f3b5fae19dab92aedc1e7b63753f33
https://doi.org/10.1002/0471264229.os096.22
https://doi.org/10.1002/0471264229.os096.22
Autor:
Hélène Lebel, Calvine Lai
Publikováno v:
Helvetica Chimica Acta. 105
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4d207b23a1b85c21a7b1c7f404789da
https://doi.org/10.1002/hlca.202100209
https://doi.org/10.1002/hlca.202100209
Autor:
Guillaume, Reynard, Hélène, Lebel
Publikováno v:
The Journal of organic chemistry. 86(17)
A new alkylation reaction of monosubstituted tetrazoles via the diazotization of aliphatic amines is reported. This method enables preferential formation of 2,5-disubstituted tetrazoles. A one-pot 1,3-dipolar cycloaddition/diazotization sequence star
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::226c28f6f39d916c0bfa2bf559bab031
https://pubmed.ncbi.nlm.nih.gov/34479404
https://pubmed.ncbi.nlm.nih.gov/34479404