Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Franck Torricelli"'
Autor:
Martina Austeri, Renaud Bach, Nathalie Mehanna, Ankit Sharma, Franck Torricelli, Walid Zeghida, Jérôme Lacour
Publikováno v:
CHIMIA, Vol 62, Iss 11 (2008)
Externí odkaz:
https://doaj.org/article/532cd6f140834003bbc1f68d2f960bbb
Autor:
Martini Austeri, Renaud Bach, Nathalie Mehanna, Roman Novikov, Ankit Sharma, Franck Torricelli, Jérôme Lacour
Publikováno v:
CHIMIA, Vol 62, Iss 1-2 (2008)
Externí odkaz:
https://doaj.org/article/176439d5577f42e9827e8c5b5ef3fbc2
Autor:
Martini Austeri, Renaud Bach, Nathalie Mehanna, Roman Novikov, Ankit Sharma, Franck Torricelli, Jérôme Lacour
Publikováno v:
CHIMIA, Vol 61, Iss 12 (2007)
Externí odkaz:
https://doaj.org/article/989924e70cd94bbbafbc950c598535a5
Autor:
Martina Austeri, David Linder, Nathalie Mehanna, Roman Novikov, Franck Torricelli, Jérôme Lacour
Publikováno v:
CHIMIA, Vol 61, Iss 10 (2007)
Externí odkaz:
https://doaj.org/article/5ea83d19ad954926b063b373be99ae49
Autor:
Sergio Abbate, Giovanna Longhi, France Lebon, Ettore Castiglioni, Stefano Superchi, Laura Pisani, Francesca Fontana, Franck Torricelli, Tullio Caronna, Claudio Villani, Rocchina Sabia, Matteo Tommasini, Andrea Lucotti, Daniele Mendola, Andrea Mele, David A. Lightner
Four different hexahelicenes, 5-aza-hexahelicene (1), hexahelicene (2), 2-methyl-hexahelicene (3), and 2-bromo-hexahelicene (4), were prepared and their enantiomers, which are stable at r.t., were separated. Vibrational circular dichroism (VCD) spect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48b5a74d042cfc77abbc6099a8ca069b
http://hdl.handle.net/11573/538458
http://hdl.handle.net/11573/538458
Autor:
Johann Bosson, Céline Besnard, Jérôme Lacour, Thomas Bürgi, Mahshid Chekini, Franck Torricelli
Publikováno v:
Angewandte Chemie: International Edition, Vol. 52, No 6 (2013) pp. 1796-1800
Angew. Chem. Int. Ed.
Angewandte Chemie-International Edition
Angew. Chem. Int. Ed.
Angewandte Chemie-International Edition
Pick and choose: Novel cationic diaza-, azaoxo-, and dioxo[6]helicenes are readily prepared and functionalized selectively by orthogonal aromatic electrophilic and vicarious nucleophilic substitutions (see scheme). Reductions, cross-coupling, or cond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7b9c79b56cc7f8348da8c613683e6b7
https://pubmed.ncbi.nlm.nih.gov/23288862
https://pubmed.ncbi.nlm.nih.gov/23288862