Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Antonio Saba"'
Publikováno v:
Chemical Engineering Transactions, Vol 98 (2023)
The focus of this paper is to critically analyse and draw quantitative balance indicators of several projects concerning process optimization, resources, and energy recovery from dairies wastes. Analysed quantitative data were collected by auditing a
Externí odkaz:
https://doaj.org/article/79ca70111029434a96ca52e7f1f1de75
Autor:
Andrea Maffini, Giorgio Bonvicini, Alessandro Venturin, Marco Morando, Antonio Saba, Bruno Fabiano
Publikováno v:
Chemical Engineering Transactions, Vol 91 (2022)
Purpose of this paper is to outline a framework for resources and energy efficiency auditing activities and present its application in field studies carried out in Italy and in Eastern Europe, to support Companies and International Financial Institut
Externí odkaz:
https://doaj.org/article/009aa96cda0e47f1b2259a1e16b5aac6
Publikováno v:
Chemical Engineering Transactions, Vol 86 (2021)
Purpose of this paper is to draw a balance of a decade of resources and energy efficiency auditing activities and studies, carried out in Eastern Europe, Central Asia and Africa, aimed to support International Financial Institutions (IFIs) in improvi
Externí odkaz:
https://doaj.org/article/098e10c676b947fb9d079954576b43e7
Autor:
Daniele Muroni, Antonio Saba
Publikováno v:
ARKIVOC, Vol 2005, Iss 13, Pp 1-7 (2005)
Externí odkaz:
https://doaj.org/article/526b34c3374e483ba02b74518f8faa95
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 7, Pp o2224-o2225 (2012)
The structure determination confirms the stereochemistry of the title compound, C21H35NO3, obtained as an intermediate in the enantioselective synthesis of deoxynojirimicine analogs. The system contains a pyrrolo[1,2-a]azocine backbone, which was syn
Externí odkaz:
https://doaj.org/article/bb249542753145dda6bf437d68bb01ad
Publikováno v:
Tetrahedron: Asymmetry. 20:1154-1159
Concise syntheses of novel chiral pyrroloazacyclo and chiral tricyclic isoquinoline alkaloids, starting from the readily available (S)-1,2,3,4-tetrahydroisoquinoline carboxylic acid methyl ester, by utilizing cascade spiro-to fused and RCM protocols,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8e9fe589117e9436fb49437988479cc
https://doi.org/10.1016/j.tetasy.2009.04.003
https://doi.org/10.1016/j.tetasy.2009.04.003
Publikováno v:
Tetrahedron Letters. 49:2373-2376
RCM approach to hindered 5-5-fused bicyclic pyrrolizidine system starting from chiral pyrrolidine, obtained from D-(+)-mannose, has been achieved in convenient yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d3daa7d7023fe287b7f9f5a106c1e93
https://doi.org/10.1016/j.tetlet.2008.02.071
https://doi.org/10.1016/j.tetlet.2008.02.071
Publikováno v:
Tetrahedron. 63:12232-12238
A concise synthesis of the novel pyrrolo[1,2-a]benzodiazepine system, by using the metallo carbenoid/spiro-[6,5]-ammonium ylide/Stevens[1,2]-shift with ring-expansion approach, was reported. The overall cascade process resulted stereospecific.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f19693690d18c1a8d0612ca6fd01309
https://doi.org/10.1016/j.tet.2007.09.062
https://doi.org/10.1016/j.tet.2007.09.062
Publikováno v:
Tetrahedron (Oxf., Print) 62 (2006): 1459–1466. doi:10.1016/j.tet.2005.11.020
info:cnr-pdr/source/autori:D. Muroni ; A. Saba ; N. Culeddu/titolo:Stable chiral spirocyclic [5,5]-ammonium ylides using a metallo carbenoid approach/doi:10.1016%2Fj.tet.2005.11.020/rivista:Tetrahedron (Oxf., Print)/anno:2006/pagina_da:1459/pagina_a:1466/intervallo_pagine:1459–1466/volume:62
info:cnr-pdr/source/autori:D. Muroni ; A. Saba ; N. Culeddu/titolo:Stable chiral spirocyclic [5,5]-ammonium ylides using a metallo carbenoid approach/doi:10.1016%2Fj.tet.2005.11.020/rivista:Tetrahedron (Oxf., Print)/anno:2006/pagina_da:1459/pagina_a:1466/intervallo_pagine:1459–1466/volume:62
Enantiomerically pure spiro[5,5]-ammonium ylides were obtained by Rh(II)-catalyzed decomposition of alfa-diazo-beta-carbonylesters. In the crude decomposition mixtures, variable quantities of enamino-alfa,beta-keto esters were detected as secondary p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3362fa5f8d5bc7d812b3e3f59386da0
https://doi.org/10.1016/j.tet.2005.11.020
https://doi.org/10.1016/j.tet.2005.11.020