Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Andrei Dragan"'
Autor:
Thomas C. Nugent, Richard Vaughan Williams, Andrei Dragan, Alejandro Alvarado Méndez, Andrei V. Iosub
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 2103-2112 (2013)
The default explanation for good to high diastereomeric excess when reducing N-chiral imines possessing only mediocre cis/trans-imine ratios (>15% cis-imine) has invariably been in situ cis-to-trans isomerization before reduction; but until now no st
Externí odkaz:
https://doaj.org/article/4a0476e71fbe40d6acfafb31e019c6e8
Autor:
Andrei Dragan
Publikováno v:
Asian Journal of Organic Chemistry. 10:3-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::800641cad9fc0410b4f1ed892b43e4f8
https://doi.org/10.1002/ajoc.202000649
https://doi.org/10.1002/ajoc.202000649
Autor:
Dhouha Ayed, Paul-Andrei Dragan, Edith Felix, Zoltan Adam Mann, Eliot Salant, Robert Seidl, Anestis Sidiropoulos, Steve Taylor, Ricardo Vitorino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da4a56c7e2a0b4c1ad0dba22a21baee4
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85135753729
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85135753729
Autor:
Andrei Dragan
Publikováno v:
Asian Journal of Organic Chemistry. 9:3-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cb342bd5d8cf67d8cc134b164018a38
https://doi.org/10.1002/ajoc.201900698
https://doi.org/10.1002/ajoc.201900698
Autor:
Dinesh Talwar, Andrei Dragan
Publikováno v:
Asian Journal of Organic Chemistry. 8:3-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6ba1cd0be0049944ff56d358b41d1fc
https://doi.org/10.1002/ajoc.201800689
https://doi.org/10.1002/ajoc.201800689
Publikováno v:
Tetrahedron. 71:8155-8161
A novel method for the Baeyer–Villiger oxidation of ketones has been developed and optimized. The transformation involves a transition metal-free activation of hydrogen peroxide under Payne epoxidation conditions. Reaction of a ketone with hydrogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfea2e3779e52f8c2d418db665cfeb03
https://doi.org/10.1016/j.tet.2015.08.037
https://doi.org/10.1016/j.tet.2015.08.037
Publikováno v:
ChemInform. 47
The products are formed as mixtures of E/Z isomers only the major isomer of which is isolated in moderate to high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::322e2dd06cd4daa6c8b22b240dacd9b4
https://doi.org/10.1002/chin.201646117
https://doi.org/10.1002/chin.201646117
Publikováno v:
Organic letters. 18(13)
The N,O-diacylhydroxylamine derivative 4 has been prepared and its reactivity with nucleophiles investigated. On reaction with lithium enolates of cyclic or acyclic ketones, 4 is converted stereoselectively to the corresponding alkylidene phthalide.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::facf24d9abce25cc5857f2ffee1b9d6d
https://pubmed.ncbi.nlm.nih.gov/27311815
https://pubmed.ncbi.nlm.nih.gov/27311815
Publikováno v:
ChemInform. 47
The novel method for the Baeyer—Villiger oxidation of ketones involves a transition metal-free activation of H2O2 under Payne epoxidation conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df8c581e9de44233e1db37ba6d4149b3
https://doi.org/10.1002/chin.201603058
https://doi.org/10.1002/chin.201603058