Zobrazeno 1 - 10
of 176
pro vyhledávání: '"Alessandro Degl'Innocenti"'
Publikováno v:
ARKIVOC, Vol 2000, Iss 4, Pp 452-466 (2000)
Externí odkaz:
https://doaj.org/article/78850caecbf8448ea9e9e50299c4059b
Autor:
Damiano Tanini, Giulia Barchielli, Antonella Capperucci, Francesca Benelli, Alessandro Degl'Innocenti
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 190:1265-1270
Aziridines react efficiently with bis(trimethyl)silyl-sulfide and -selenide to afford a direct access to β-amino thiols and selenols. Synthesis of 2,4-disubstituted 1,3-selenazolidines is obtained ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d01f2c2d8b0b066c36086fd564e21519
https://doi.org/10.1080/10426507.2014.1002615
https://doi.org/10.1080/10426507.2014.1002615
Publikováno v:
European Journal of Organic Chemistry. 2015:357-369
A novel approach to the synthesis of β-substituted dialkyl diselenides and selenides is described through reaction of bis(trimethylsilyl)selenide with epoxides, thiiranes, and aziridines catalyzed by tetrabutylammonium fluoride. Selective formation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85eaf3a65ea28deef7f4c0abcb2883cb
https://doi.org/10.1002/ejoc.201403015
https://doi.org/10.1002/ejoc.201403015
Autor:
Jose Luis Garcia Ruano, Antonella Capperucci, Inés Alonso, Ana M. Martín-Castro, Alessandro Degl'Innocenti, Esther Torrente, Lucrezia Frateschi, Mercedes Rodriguez
Publikováno v:
The Journal of Organic Chemistry. 77:1974-1982
Phenylselenyl benzylcarbanion stabilized by an (S)-2-p-tolylsulfinyl group evolves in a highly stereoselective way in the reactions with (S)-N-(p-tolylsulfinyl)imines at -98 °C affording diastereomerically pure 1,2-selenoamino derivatives in good yi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e4c8c7992af1b7ef7784c7f98b56912
https://doi.org/10.1021/jo202611v
https://doi.org/10.1021/jo202611v
Publikováno v:
Synlett. 2011:2248-2252
Reaction of acyl chlorides with phenylselenotrimethylsilane promoted by TBAF afforded a mild general access to selenolesters in good yields. When acyl chlorides were reacted with bis(trimethylsilyl)selenide (HMDSS) in 2:1 or 1:1 ratio a selective e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::298b6be15040ad61d978b31ba8bf8fc7
https://doi.org/10.1055/s-0030-1261195
https://doi.org/10.1055/s-0030-1261195
Autor:
Raffaella Terlizzi, Andrea Temperini, Antonella Capperucci, Marcello Tiecco, Alessandro Degl'Innocenti
Publikováno v:
Tetrahedron Letters. 51:4121-4124
A method for the synthesis of β3-amino acids starting from α-amino acids is described. This conversion can be effected by an eight-step procedure which involves the transformation of the carboxylic group into an alkyne followed by a selenium-mediat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe79a30539d16b443b908aee9a6611f4
https://doi.org/10.1016/j.tetlet.2010.05.143
https://doi.org/10.1016/j.tetlet.2010.05.143
Publikováno v:
Communications in Soil Science and Plant Analysis. 41:72-87
Recycling organic waste in agricultural soils is a valid solution. We performed short‐term experiments to investigate the fate of urban sludge and composts, in mine spoils, cultivated or uncultivated, and reclaimed soils located in Florence and Mil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01d7a123caa16a31804ab94fa83697de
https://doi.org/10.1080/00103620903360288
https://doi.org/10.1080/00103620903360288
Publikováno v:
Journal of Sulfur Chemistry. 30:319-326
Fluoride-ion-induced reactivity of bromo(phenylthio)methyltrimethylsilane with o-hydroxy benzaldehyde and o-mercaptobenzyl alcohol afforded direct and simple access to 2,3-dihydro-2-phenylthio-3-hydroxybenzofuran and 2-phenylthio-3-hydroxy-2,3-dihydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b544862cb9cc5219c53423d8552d2cdf
https://doi.org/10.1080/17415990902998587
https://doi.org/10.1080/17415990902998587
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 184:1621-1626
Bis(trimethylsilyl)selenide (HMDSS) reacts efficiently with aldehydes in the presence of CoCl 2 .6H 2 O to afford selenoaldehydes, which are trapped as Diels–Alder adducts by different dienes. The reaction can be applied to acylsilanes, to afford s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52aef6032d373953959c5bdc68d0127e
https://doi.org/10.1080/10426500902947989
https://doi.org/10.1080/10426500902947989
Autor:
Caterina Tiberi, Brunella Innocenti, Irene Malesci, Alessandro Degl'Innocenti, Antonella Capperucci, Giulio Castagnoli
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 183:966-969
Bis(trimethylsilyl)selenide (HMDSS) acts as an efficient reagent in the TBAF catalyzed reaction with different substituted epoxides, episulfides, and aziridines, leading to β -functionalized diselenides in a highly regio- and stereoselective way. Wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e093fd790730500e2edd990e8d532544
https://doi.org/10.1080/10426500801900923
https://doi.org/10.1080/10426500801900923