A two-step one purification access to dichloronaphtho[1,2-b:8,7-b′] and [1,2-b:5,6-b′]dithiophenes using bis-alkylnaphthyl alkynes and phthalimidesulfenyl chloride as starting materials has been developed. The functionalization of the carbon-chlorine bonds allowed further modification of NDT core, broadening the potential of the methodology. © 2013 American Chemical Society.
Regioselective Electrophilic Access to Naphtho[1,2-b:8,7-b′]- and -[1,2-b:5,6-b′]dithiophenes / Caterina, Viglianisi; Lucia, Becucci; Faggi, Cristina; Sara, Piantini; Piero, Procacci; Stefano, Menichetti. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 78:(2013), pp. 3496-3502. [10.1021/jo400205j]
Regioselective Electrophilic Access to Naphtho[1,2-b:8,7-b′]- and -[1,2-b:5,6-b′]dithiophenes
VIGLIANISI, CATERINA;BECUCCI, LUCIA;FAGGI, CRISTINA;PIANTINI, SARA;PROCACCI, PIERO;MENICHETTI, STEFANO
2013
Abstract
A two-step one purification access to dichloronaphtho[1,2-b:8,7-b′] and [1,2-b:5,6-b′]dithiophenes using bis-alkylnaphthyl alkynes and phthalimidesulfenyl chloride as starting materials has been developed. The functionalization of the carbon-chlorine bonds allowed further modification of NDT core, broadening the potential of the methodology. © 2013 American Chemical Society.File | Dimensione | Formato | |
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