메뉴 건너뛰기




Volumn , Issue 2, 2013, Pages 217-227

Thienannulation: Efficient synthesis of π-extended thienoacenes applicable to organic semiconductors

Author keywords

Annulation; Materials science; Molecular electronics; Organic field effect transistors; Selenium; Semiconductors; Sulfur heterocycles

Indexed keywords


EID: 84871894729     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201201139     Document Type: Review
Times cited : (75)

References (104)
  • 64
    • 84865211657 scopus 로고    scopus 로고
    • The Synthesis characterization, and FET device characteristics of isomerically pure syn-and anti-dimethyl-ADTs were reported during the preparation of this manuscript, see:, M. Mamada, T. Minamiki, H. Katagiri, S. Tokito, Org. Lett. 2012, 14, 4062.
    • (2012) Org. Lett. , vol.14 , pp. 4062
    • Mamada, M.1    Minamiki, T.2    Katagiri, H.3    Tokito, S.4
  • 98
    • 84868246665 scopus 로고    scopus 로고
    • Recently, largely π-extended thienoacenes with two internal thieno[3,2-b]thiophene substructures have been synthesized by a double iodine-promoted thienothiophene formation reaction. See
    • Recently, largely π-extended thienoacenes with two internal thieno[3,2-b]thiophene substructures have been synthesized by a double iodine-promoted thienothiophene formation reaction. See, T. Yamamoto, T. Nishimura, T. Mori, E. Miyazaki, I. Osaka, K. Takimiya, Org. Lett. 2012, 14, 4914.
    • (2012) Org. Lett. , vol.14 , pp. 4914
    • Yamamoto, T.1    Nishimura, T.2    Mori, T.3    Miyazaki, E.4    Osaka, I.5    Takimiya, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.