Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Davide Baraldi"'
Publikováno v:
Synthetic Communications. 29:3125-3135
This paper deals with a novel and versatile synthetic approach for the introduction of a functionalized ethynyl side chain at the C-3 position of the 2-carboxyindole nucleus. The key step of this process is represented by the coupling reaction betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b490df48d566dca9e939306dd86ad1fc
https://doi.org/10.1080/00397919908085936
https://doi.org/10.1080/00397919908085936
Publikováno v:
ChemInform. 23
Adducts AlCl 3 .RCOC1 undergo highly regioselective self- and cross-condensation. 4-Hydroxy-2-pyrones and 2-acetyl-indan-1,3-diones are synthesized in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce06916387c02b64dccee4950ced31c8
https://doi.org/10.1002/chin.199207176
https://doi.org/10.1002/chin.199207176
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::173871212d1d427538cb98e40e85ea05
https://doi.org/10.1002/chin.199310180
https://doi.org/10.1002/chin.199310180
Autor:
Xiaochun Tao, Franca Bigi, Giuseppe Casnati, Davide Baraldi, Giovanni Sartori, Raimondo Maggi
Publikováno v:
ChemInform. 25
The synthesis of a series of persubstituted 4-hydroxy-2-pyrones 6 by regioselective «one-pot» cyclotrimerization of aliphatic acyl chlorides promoted by aluminum chloride is reported
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db1cdaea1cddb2585637d822aa294b22
https://doi.org/10.1002/chin.199406151
https://doi.org/10.1002/chin.199406151
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c013eea0ecf8fb39ea27b669d0c6a77
https://doi.org/10.1002/chin.199844124
https://doi.org/10.1002/chin.199844124
Publikováno v:
ChemInform. 30
This paper deals with a novel and versatile synthetic approach for the introduction of a functionalized ethynyl side chain at the C-3 position of the 2-carboxyindole nucleus. The key step of this process is represented by the coupling reaction betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53511e50f76252843e6e9420648f58e7
https://doi.org/10.1002/chin.199947145
https://doi.org/10.1002/chin.199947145
Autor:
Davide Baraldi, Paola Gastaldi, Alfredo Cugola, Daniele Donati, Simone Giacobbe, Gianluca Araldi, Giorgio Pentassuglia, Romano Di Fabio, Fabrizio Micheli
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ee36195b4688d09335e7af0afdc4a47
https://doi.org/10.1002/chin.200207107
https://doi.org/10.1002/chin.200207107
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2985-2988
Variously substituted indan-1,3-diones have been regioselectively prepared in a one-pot synthesis by sequential cross-condensation–cycloacylation of aromatic acyl chlorides and acetyl chloride or malonyl dichloride, electrophilic acylation of aroma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8198a365a67e2e3ed23745a99619f080
https://doi.org/10.1039/p19920002985
https://doi.org/10.1039/p19920002985
Publikováno v:
Tetrahedron Letters. 32:2153-2156
Adducts AlCl 3 .RCOC1 undergo highly regioselective self- and cross-condensation. 4-Hydroxy-2-pyrones and 2-acetyl-indan-1,3-diones are synthesized in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31bf19ae43d675efbbdd74d80fb344a2
https://doi.org/10.1016/s0040-4039(00)71262-7
https://doi.org/10.1016/s0040-4039(00)71262-7
Autor:
Daniele Donati, Paola Gastaldi, Romano Di Fabio, Simone Giacobbe, Alfredo Cugola, Gianluca Araldi, Davide Baraldi, Giorgio Pentassuglia, Fabrizio Micheli
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 56(10)
After the identification of GV150526, the indole-2-carboxylate template was further explored in order to identify novel potential anti-stroke agents. In particular, the SAR of the side chain present at the C-3 position of the indole nucleus was widel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2daec2fd265b956fa283791a71bf265
https://pubmed.ncbi.nlm.nih.gov/11718273
https://pubmed.ncbi.nlm.nih.gov/11718273