18684-88-3Relevant articles and documents
Total synthesis and DNA-cleaving properties of thiarubrine C
Wang, Yamin,Koreeda, Masato,Chatterji, Tonika,Gates, Kent S.
, p. 8644 - 8645 (1998)
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Synthesis of 1,5-diphenylpent-3-en-1-yne derivatives utilizing an aqueous B-alkyl Suzuki cross coupling reaction
Chuang, Da-Wei,El-Shazly, Mohamed,Chen, Chin-Chau,Chung, Yu-Ming,D. Barve, Balaji,Wu, Ming-Jung,Chang, Fang-Rong,Wu, Yang-Chang
supporting information, p. 5162 - 5166 (2013/09/02)
1,5-Diphenylpent-3-en-1-yne derivatives were isolated in minor quantities from terrestrial plants and exhibited strong anti-inflammatory activity. A cross coupling reaction between B-benzyl-9-BBN and chloroenynes under mild condition was developed resulti
Substituent effects on the cyclization mode of 7-sulfonyl-3-hepten-1,5- diynes and 11-sulfonylundeca-3,7-dien-1,5,9-triynes
Wu, Huey-Juan,Lin, Chi-Fong,Lee, Jeng-Lin,Lu, Wen-Der,Lee, Chia-Ying,Chen, Chin-Chau,Wu, Ming-Jung
, p. 3927 - 3934 (2007/10/03)
In probing of cycloaromatization of 7-phenylsulfonyl-3-hepten-1,5-diyne systems to generate biradical intermediates under an alkaline condition suggested that the aryl moiety on C3-C4 also plays an important role to switch the Myers cyclization to Schmitt