Modular Synthesis of Planar-Chiral para-Substituted Paracyclophanes by Double Suzuki Coupling

Çakıcı, Murat; BRAESE, Stefan

doi:10.1002/ejoc.201201043

Makale Tam Makale Uluslararası 2012

Modular Synthesis of Planar-Chiral para-Substituted Paracyclophanes by Double Suzuki Coupling

Murat Çakıcı, Stefan BRAESE

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY Sayı 31 · ss. 6132–6135 · 01.11.2012

DOI ile aç

Özet

The first synthesis of enantiomerically pure 4,7-paracyclophane ditriflate starting from a quinone was reported. Using this molecule, mono- or dicoupling with boronic acids delivered enantiomerically pure arylparacyclophanes.

Anahtar kelimeler

DERIVATIVES Boron Chirality Cyclophanes Cross-coupling Hydrocarbons MACRO RINGS

Atıf için künye

Çakıcı, M., & BRAESE, S. (2012). Modular Synthesis of Planar-Chiral para-Substituted Paracyclophanes by Double Suzuki Coupling. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY(31), 6132–6135. https://doi.org/10.1002/ejoc.201201043

BibTeX

@article{cakici2012-72649,
  author = {Çakıcı, Murat and BRAESE, Stefan},
  title = {Modular Synthesis of Planar-Chiral para-Substituted Paracyclophanes by Double Suzuki Coupling},
  journal = {EUROPEAN JOURNAL OF ORGANIC CHEMISTRY},
  year = {2012},
  number = {31},
  pages = {6132--6135},
  issn = {1434-193X},
  doi = {10.1002/ejoc.201201043},
  url = {https://akademik.atauni.edu.tr/yayinlar/72649-modular-synthesis-of-planar-chiral-para-substituted-paracyclophanes-by-double}
}