Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Luigi Longobardo"'
Autor:
Marina DellaGreca, Luigi Longobardo
Hydroxycinnamic acids such as p-coumaric, ferulic, sinapic and caffeic acids were protected as carbonates and activated as mixed carbonic anhydrides in water at RT by adding a base and isobutyl chloroformate. These anhydrides were used for amine and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9abe0882e632f83410efb5090fe343da
http://hdl.handle.net/11588/803616
http://hdl.handle.net/11588/803616
Publikováno v:
ChemistrySelect. 3:10637-10640
A novelprocedurefor reductionandsimultaneousprotectionof phenolgroupsof hydroxycinnamicacidsto therelatedalcoholshas beendeveloped.Duringthe formationof mixedanhydridesfromtheacidsandan alkylchloroformate,thephenolwasprotectedas carbonate,andthe mixe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef1dfa8a55909ca92801be73c27315c
https://doi.org/10.1002/slct.201802099
https://doi.org/10.1002/slct.201802099
Publikováno v:
Amino Acids. 44:443-448
Natural L-homocysteine and L,L-cystathionine, along with a series of unnatural analogues, have been prepared from L-aspartic and L-glutamic acid. Manipulation of the protected derivatives provided ω-iodoamino acids, which were used in thioalkylation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbb62618f2cdb7f73c2c32d751fffe7b
https://doi.org/10.1007/s00726-012-1352-5
https://doi.org/10.1007/s00726-012-1352-5
Publikováno v:
Europe PubMed Central
Developing seeds from Triticum aestivum (wheat) cultivars were collected after flowering and analysed for puroindoline a and b gene expression by Real Time RT-PCR. Mature seeds were investigated for the presence and the amount of starch-associated pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02e9b7b679cdedde630b4ec6813f2c98
https://doi.org/10.1007/s10529-004-3745-3
https://doi.org/10.1007/s10529-004-3745-3
Autor:
Filomena Tafuro, Francesco Addeo, Dominique Melck, Pasquale Ferranti, Gianfranco Mamone, Lina Chianese, Luigi Longobardo
Publikováno v:
FEBS Letters. 562:177-182
A peptidomics approach was developed to identify transglutaminase-susceptible Q residues within a pepsin-trypsin gliadin digest. Based on tagging with a monodansylcadaverine fluorescent probe, six alpha/beta-, gamma-gliadin, and low molecular weight
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb95def78f0445585f0b9fd40ee98dbc
https://doi.org/10.1016/s0014-5793(04)00231-5
https://doi.org/10.1016/s0014-5793(04)00231-5
Autor:
Luigi Longobardo, Giancarlo Cammarota, Dominique Melck, Rosa Siciliano, Antonello Santini, Vincenzo Di Marzo
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 10:1185-1188
Two analogues of bovine beta-casomorphin-7 and beta-casomorphin-5 containing a beta-homo phenylalanine in substitution of the phenylalanine in position 3 were synthesised and tested for their mu-opioid receptor affinity. The modification enhanced the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb7362cc3723cf9efffeb25846c5322e
https://doi.org/10.1016/s0960-894x(00)00187-6
https://doi.org/10.1016/s0960-894x(00)00187-6
Publikováno v:
Tetrahedron Letters. 48:1425-1427
The general synthesis of a new class of non-natural diamino acids, 2-amino-3-[(2′-aminoalkyl)seleno]propanoic acids, or Se-(aminoalkyl)selenocysteines, is reported. Under the conditions devised, enantiopure N -Boc-protected β- l -iodoamines, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60c4c8fd0482e25ed00b60ca5baff2b0
https://doi.org/10.1016/j.tetlet.2006.12.096
https://doi.org/10.1016/j.tetlet.2006.12.096
Publikováno v:
Tetrahedron. 52:11857-11866
A new strategy is designed to synthesize polyhydroxyl compounds (and/or carbohydrates) by coupling of 5,6-dihydro-1,4-dithiins - carrying a vinylic hydrogen atom - with chiral aldehydes and, in sequence, stereoselective removal of the dithiodimethyle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ecd341a7e5db80fafffeec63cf1c567
https://doi.org/10.1016/0040-4020(96)00677-1
https://doi.org/10.1016/0040-4020(96)00677-1
Publikováno v:
Scopus-Elsevier
Ketones are reported to be conveniently converted into their α-tolylsulfinylated derivatives. This new procedure is based on the reaction of their corresponding trimethylsilyl enol ethers with p-toluenesulfinyl p-tolylsulfone in the presence of tris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa3b0f192ad3e4d7c02123502cccc341
https://doi.org/10.1080/00397919308011245
https://doi.org/10.1080/00397919308011245
Publikováno v:
ChemInform. 22
The stereoselectivity of the Lewis acid induced acylation of open-chain silyl enoi ethers by chiral orthoesters is strongly affected by the CC bond configuration: both Z and E silyl enol ethers are acylated in good isolated yields, but the Z isomers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c72edab0588b287223ed1429f4cf037
https://doi.org/10.1002/chin.199134129
https://doi.org/10.1002/chin.199134129