Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marco Lumini"'
Autor:
Alfonso Carotenuto, Anna Maria Papini, Diego Brancaccio, Giuseppina Sabatino, Samuele Stazzoni, Marco Chinol, Mauro Ginanneschi, Paolo Rovero, Marco Lumini, Alessandro Pratesi, Ettore Novellino
Publikováno v:
Chemical engineering and processing
122 (2017): 365–372. doi:10.1016/j.cep.2017.02.005
info:cnr-pdr/source/autori:Pratesi A.; Stazzoni S.; Lumini M.; Sabatino G.; Carotenuto A.; Brancaccio D.; Novellino E.; Chinol M.; Rovero P.; Ginanneschi M.; Papini A.M./titolo:Synthesis of dicarba-cyclooctapeptide Somatostatin analogs by conventional and MW-assisted RCM: A study about the impact of the configuration at C? of selected amino acids/doi:10.1016%2Fj.cep.2017.02.005/rivista:Chemical engineering and processing (Print)/anno:2017/pagina_da:365/pagina_a:372/intervallo_pagine:365–372/volume:122
122 (2017): 365–372. doi:10.1016/j.cep.2017.02.005
info:cnr-pdr/source/autori:Pratesi A.; Stazzoni S.; Lumini M.; Sabatino G.; Carotenuto A.; Brancaccio D.; Novellino E.; Chinol M.; Rovero P.; Ginanneschi M.; Papini A.M./titolo:Synthesis of dicarba-cyclooctapeptide Somatostatin analogs by conventional and MW-assisted RCM: A study about the impact of the configuration at C? of selected amino acids/doi:10.1016%2Fj.cep.2017.02.005/rivista:Chemical engineering and processing (Print)/anno:2017/pagina_da:365/pagina_a:372/intervallo_pagine:365–372/volume:122
This work describes the synthesis of thirteen cyclooctapeptides dicarba-analogues of Somatostatin, containing l- or d-allylglycine (Agl) residues at the termini of the peptide chain, through on resin Ring Closing Metathesis (RCM) of the linear octape
Autor:
Ettore Novellino, Mauro Ginanneschi, Alfonso Carotenuto, Marco Lumini, Anna Maria Papini, Alessandro Pratesi, Diego Brancaccio
Publikováno v:
Frontiers in Chemistry
In vivo somatostatin receptor scintigraphy is a valuable method for the visualization of human endocrine tumours and their metastases. In fact, peptide ligands of somatostatin receptors (sst’s) conjugated with chelating agents are in clinical use.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b58de59de43c2ea64f06a64aeef361b
http://hdl.handle.net/11588/679631
http://hdl.handle.net/11588/679631
Publikováno v:
European Journal of Organic Chemistry. 2008:2817-2824
The synthesis of several α-substituted N-Boc-protected prolines has been achieved by cross metathesis (CM) of N-Boc-allylproline 5 with terminal long chain alkenes and alkenes bearing hydroxy, silyloxy, ester, and O-acetylglucosamido groups. The CM
Publikováno v:
Synlett. 2007:2882-2884
The synthesis of α-substituted prolines has been accomplished by microwave-assisted Huisgen 1,3-dipolar cycloaddition between azides and orthogonally protected α-propynyl proline in the presence of Cu(I).
Publikováno v:
ChemInform. 39
The synthesis of several α-substituted N-Boc-protected prolines has been achieved by cross metathesis (CM) of N-Boc-allylproline 5 with terminal long chain alkenes and alkenes bearing hydroxy, silyloxy, ester, and O-acetylglucosamido groups. The CM
Publikováno v:
ChemInform. 39
The synthesis of α-substituted prolines has been accomplished by microwave-assisted Huisgen 1,3-dipolar cycloaddition between azides and orthogonally protected α-propynyl proline in the presence of Cu(I).