| Makale Türü |
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| Dergi Adı | Helvetica Chimica Acta (Q1) | ||
| Dergi ISSN | 0018-019X Dergi Bilgileri (2003) | ||
| Dergi Tarandığı Indeksler | SSCI | ||
| Makale Dili | İngilizce | Basım Tarihi | 10-2003 |
| Kabul Tarihi | – | Yayınlanma Tarihi | 01-10-2003 |
| Cilt / Sayı / Sayfa | 86 / 10 / 3332–3341 | DOI | 10.1002/hlca.200390276 |
| Makale Linki | http://doi.wiley.com/10.1002/hlca.200390276 | ||
| UAK Araştırma Alanları |
Organik Kimya
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| Özet |
| AbstractThe addition of benzyne to trans‐7,8‐dibromobicyclo[4.2.0]octa‐2,4‐diene (6) led to the formation of dibromide 7. The dehydrobromination of 7 followed by replacement of the Br‐atom with a CN substituent gave 9. Photolysis of 9 in acetone at 254 nm yielded the desired monosubstituted benzobasketene derivative 10. Bromination of monobromide 8 followed by dehydrobromination furnished the symmetrically substituted dibromo compound 15. Further bromination of 7 followed by dehydrobromination resulted in the formation of the dibromides 20 and 21. Substitution of the Br‐atoms in 15, 20, and 21 with CN substituents and photolysis of the formed dicarbonitriles 16, 23, and 24 gave the target benzobasketene‐dicarbonitriles 17, 25, and 26, respectively. |
| Anahtar Kelimeler |
| Dergi Adı | HELVETICA CHIMICA ACTA |
| Kısa Adı | HELV CHIM ACTA |
| Yayıncı | WILEY-V C H VERLAG GMBH |
| Açık Erişim | Hayır |
| ISSN | 0018-019X |
| E-ISSN | 1522-2675 |
| Wos Quartile | Q1 |
| Scopus Quartile | Q1 |
| Tarandığı Indeksler | SCIE , Scopus |
| WoS Kategoriler | CHEMISTRY, MULTIDISCIPLINARY |
| Scopus Kategoriler | DRUG DISCOVERY | INORGANIC CHEMISTRY | ORGANIC CHEMISTRY | BIOCHEMISTRY | PHYSICAL AND THEORETICAL CHEMISTRY | CATALYSIS |