Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Maria Bucciarelli"'
Publikováno v:
ARKIVOC, Vol 2002, Iss 11, Pp 45-53 (2002)
Externí odkaz:
https://doaj.org/article/5218871294114e3bbd0054055f560d6d
Publikováno v:
Il Farmaco. 58:1029-1032
Levodropropizine, an antitussive drug, was prepared in high enantiomeric excess in three steps, starting from dichloroacetone (2). Monosubstitution of 2 with sodium benzoate and subsequent baker's yeast reduction stereoselectively afforded the corres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4451be64a460685d48e34ada926f394c
https://doi.org/10.1016/s0014-827x(03)00189-7
https://doi.org/10.1016/s0014-827x(03)00189-7
Publikováno v:
ARKIVOC, Vol 2002, Iss 11, Pp 45-53 (2002)
Scopus-Elsevier
Scopus-Elsevier
Reduction with baker's yeast of ethyl or methyl 4-chloro-3-oxobutanoate in the presence of allyl bromide or allyl alcohol as additive afforded the corresponding L- and D-3-hydroxyesters. Several reduction conditions were tested, involving: different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c8755dbba8b1ecef9c01b6596da9891
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0003.b06
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0003.b06
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1948-1953
The Amano PS lipase-catalyzed acetylation of 2-hydroxymethylaziridines 1a–e has been investigated in order to evaluate the effect of ring substituents on the enantioselectivity of the reaction and to assess the stereochemical preference of the enzy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58fdc4dced763cec326fd2a3ed8ccb7f
https://doi.org/10.1039/b205374h
https://doi.org/10.1039/b205374h
Publikováno v:
Letters in Organic Chemistry. 4:319-321
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e78dd25b418bb631c72515295dc08aeb
https://doi.org/10.2174/157017807781212157
https://doi.org/10.2174/157017807781212157
Autor:
Irene Moretti, Maria Bucciarelli, Emilia Caselli, Fabio Prati, Giovanni Torre, Luciano Antolini, Arrigo Forni, Paolo Davoli
Publikováno v:
The Journal of Organic Chemistry. 62:8784-8789
The nucleophilic ring opening of trans-aziridine-2,3-dicarboxylate 1 and substituted N-acyl-, N-(methoxycarbonyl)-, and N-(methanesulfonyl)aziridine-2,3-dicarboxylates 2−4 allows an easy synthetic approach to β-hydroxy, β-amino, β-(alkylthio), a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb26d4272544799f15ce45ae7a2520ef
https://doi.org/10.1021/jo971285+
https://doi.org/10.1021/jo971285+
Publikováno v:
Tetrahedron: Asymmetry. 6:2073-2080
(S)-(−)-N-acetyl-2-methoxycarbonylaziridine 1 undergoes easy ring-opening by Bronsted acids or nucleophiles in the presence of a Lewis acid catalyst. The regioselectivity is not always exclusive, affording optically active α- and β-aminoacids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bddd7dbea6f0e338bdc4d1db475119be
https://doi.org/10.1016/0957-4166(95)00270-y
https://doi.org/10.1016/0957-4166(95)00270-y