Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jack T. Floreancig"'
Publikováno v:
ACS Omega, Vol 5, Iss 25, Pp 15734-15745 (2020)
Externí odkaz:
https://doaj.org/article/b3f58ef20f274d558fa2218318df0062
Publikováno v:
Org Lett
We report that the treatment of unsymmetrical 2,3-disubstituted aziridines with TiCl(4) yields β-phenethylamine products via the intermediacy of a phenonium ion. Derivatization of the products obtained via this method is demonstrated. Computational
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7eeb516247e1c2ff394325237e51a01
https://doi.org/10.1021/acs.orglett.1c03857
https://doi.org/10.1021/acs.orglett.1c03857
Autor:
Makafui Gasonoo, Sébastien Laulhé, Alexandra S. Kelley, Charles D. Irving, Jack T. Floreancig
Publikováno v:
ChemistrySelect
A deoxyamination methodology of activated and unactivated alcohols is presented. The reaction is mediated by phosphonium intermediates generated in situ from N-haloimides and triphenylphosphine. The protocol allows for the synthesis of phthalimide an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efc7c221b187aa5504c81994ee0d680f
https://doi.org/10.1002/slct.202102296
https://doi.org/10.1002/slct.202102296
Publikováno v:
ACS Omega, Vol 5, Iss 25, Pp 15734-15745 (2020)
ACS Omega
ACS Omega
We describe a methodology for the amidation of carboxylic acids by generating phosphonium salts in situ from N-chlorophthalimide and triphenylphosphine. Aliphatic, benzylic, and aromatic carboxylic acids can be transformed into their amide counter pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffad7b59aecb991bbd60b148ea358f5f
https://doi.org/10.1021/acsomega.0c02309
https://doi.org/10.1021/acsomega.0c02309
Autor:
Irving, Charles D.1 (AUTHOR), Floreancig, Jack T.1 (AUTHOR), Gasonoo, Makafui1 (AUTHOR), Kelley, Alexandra S.1 (AUTHOR), Laulhé, Sébastien1 (AUTHOR) slaulhe@iupui.edu
Publikováno v:
ChemistrySelect. 9/7/2021, Vol. 6 Issue 33, p8874-8878. 5p.