Synthesis of cyclopropane-annulated conduritol derivatives: norcaran-2,3,4,5-tetraoles

SENGUEL, Mehmet Emin; MENZEK, Abdullah; Şahin, Ertan; ARIK, Mustafa; SARAÇOĞLU, Nurullah

doi:10.1016/j.tet.2008.05.066

Makale Tam Makale Uluslararası 2008

Synthesis of cyclopropane-annulated conduritol derivatives: norcaran-2,3,4,5-tetraoles

Mehmet Emin SENGUEL, Abdullah MENZEK, Ertan Şahin, Mustafa ARIK, Nurullah SARAÇOĞLU

TETRAHEDRON Cilt 64 · ss. 7289–7294 · 21.07.2008

DOI ile aç

Özet

Norcaran-23,45-tetraoles were synthesized starting from methyl 1,3,5-cycloheptatriene-7-carboxylate in several steps. Norcaradiene endoperoxide is the key component; it was obtained by photooxygenation of methyl 1,3,5-cycloheptatriene-7-carboxylate. The other oxygen functionalities are introduced through epoxide ring opening and OSO4-hydroxylation reactions. (c) 2008 Elsevier Ltd. All rights reserved.

Atıf için künye

SENGUEL, M. E., MENZEK, A., Şahin, E., ARIK, M., & SARAÇOĞLU, N. (2008). Synthesis of cyclopropane-annulated conduritol derivatives: norcaran-2,3,4,5-tetraoles. TETRAHEDRON, 64, 7289–7294. https://doi.org/10.1016/j.tet.2008.05.066

BibTeX

@article{senguel2008-66795,
  author = {SENGUEL, Mehmet Emin and MENZEK, Abdullah and Şahin, Ertan and ARIK, Mustafa and SARAÇOĞLU, Nurullah},
  title = {Synthesis of cyclopropane-annulated conduritol derivatives: norcaran-2,3,4,5-tetraoles},
  journal = {TETRAHEDRON},
  year = {2008},
  volume = {64},
  pages = {7289--7294},
  issn = {0040-4020},
  doi = {10.1016/j.tet.2008.05.066},
  url = {https://akademik.atauni.edu.tr/yayinlar/66795-synthesis-of-cyclopropane-annulated-conduritol-derivatives-norcaran-2345}
}