Selected synthetic strategies to cyclophanes

Sambasivarao Kotha, Mukesh E. Shirbhate and Gopalkrushna T. Waghule
Beilstein J. Org. Chem. 2015, 11, 1274–1331. https://doi.org/10.3762/bjoc.11.142

Cite the Following Article

Selected synthetic strategies to cyclophanes
Sambasivarao Kotha, Mukesh E. Shirbhate and Gopalkrushna T. Waghule
Beilstein J. Org. Chem. 2015, 11, 1274–1331. https://doi.org/10.3762/bjoc.11.142

How to Cite

Kotha, S.; Shirbhate, M. E.; Waghule, G. T. Beilstein J. Org. Chem. 2015, 11, 1274–1331. doi:10.3762/bjoc.11.142

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Li, J.; Dong, Z.; Chen, Y.; Yang, Z.; Yan, X.; Wang, M.; Li, C.; Zhao, C. N-Heterocyclic carbene-catalyzed enantioselective synthesis of planar-chiral cyclophanes via dynamic kinetic resolution. Nature Communications 2024, 15. doi:10.1038/s41467-024-46376-8
  • Zhu, D.; Mu, T.; Li, Z.-L.; Luo, H.-Y.; Cao, R.-F.; Xue, X.-S.; Chen, Z.-M. Enantioselective Synthesis of Planar-Chiral Sulfur-Containing Cyclophanes by Chiral Sulfide Catalyzed Electrophilic Sulfenylation of Arenes. Angewandte Chemie (International ed. in English) 2024, 63, e202318625. doi:10.1002/anie.202318625
  • Zhu, D.; Mu, T.; Li, Z.; Luo, H.; Cao, R.; Xue, X.; Chen, Z. Enantioselective Synthesis of Planar‐Chiral Sulfur‐Containing Cyclophanes by Chiral Sulfide Catalyzed Electrophilic Sulfenylation of Arenes. Angewandte Chemie 2024, 136. doi:10.1002/ange.202318625
  • Wang, J.; Wang, M.; Wen, Y.; Teng, P.; Li, C.; Zhao, C. N-Heterocyclic Carbene-Catalyzed Highly Enantioselective Macrolactonization to Access Planar-Chiral Macrocycles. Organic letters 2024, 26, 1040–1045. doi:10.1021/acs.orglett.3c04200
  • Guo, H.; Qiu, S.; Xu, P. One‐Carbon Ring Expansion of Indoles and Pyrroles: A Straightforward Access to 3‐Fluorinated Quinolines and Pyridines. Angewandte Chemie 2023, 136. doi:10.1002/ange.202317104
  • Guo, H.; Qiu, S.; Xu, P. One-Carbon Ring Expansion of Indoles and Pyrroles: A Straightforward Access to 3-Fluorinated Quinolines and Pyridines. Angewandte Chemie (International ed. in English) 2023, 63, e202317104. doi:10.1002/anie.202317104
  • Phan, C.-S.; Morinaka, B. I. Bacterial cyclophane-containing RiPPs from radical SAM enzymes. Natural product reports 2023. doi:10.1039/d3np00030c
  • Dong, Z.; Li, J.; Yao, T.; Zhao, C. Palladium‐Catalyzed Enantioselective C−H Olefination to Access Planar‐Chiral Cyclophanes by Dynamic Kinetic Resolution. Angewandte Chemie 2023, 135. doi:10.1002/ange.202315603
  • Dong, Z.; Li, J.; Yao, T.; Zhao, C. Palladium-Catalyzed Enantioselective C-H Olefination to Access Planar-Chiral Cyclophanes by Dynamic Kinetic Resolution. Angewandte Chemie (International ed. in English) 2023, 62, e202315603. doi:10.1002/anie.202315603
  • Li, J.; Zhao, C. Highly Enantioselective Synthesis of Planar-Chiral Cyclophanes through a Brønsted Acid-Catalyzed Asymmetric Transfer Hydrogenation. ACS Catalysis 2023, 13, 14155–14162. doi:10.1021/acscatal.3c03718
  • Jayasree, E. G.; Sukumar, C. Strained thiacyclophanes: Reducing properties and gauge of transannular interactions. Journal of molecular graphics & modelling 2023, 125, 108607. doi:10.1016/j.jmgm.2023.108607
  • Kotha, S.; Chaurasia, U. N.; Jena, K. Ring‐Rearrangement Metathesis Approach to Fused [5/5/6/5/5] and [6/5/5/5/5/6] Carbocyclic Derivatives. ChemistrySelect 2023, 8. doi:10.1002/slct.202302094
  • Szcześniak, P.; Furman, B. Diversity-oriented synthesis of medium-sized cyclophanes via the photo-fries rearrangement of N-aryl lactams. Reaction Chemistry & Engineering 2023, 8, 1923–1929. doi:10.1039/d3re00193h
  • Kawai, Y.; Nogami, J.; Nagashima, Y.; Tanaka, K. Stereoselective synthesis of [2.2]triphenylenophanes via intramolecular double [2 + 2 + 2] cycloadditions. Chemical science 2023, 14, 3963–3972. doi:10.1039/d3sc00571b
  • Kotha, S.; Salman, M.; Lal, S.; Rao Cheekatla, S.; Ansari, S. Design and Synthesis of Nitro Cage Heterocycles as Energetic Materials Derived from Pentacycloundecane (PCUD) Systems. Asian Journal of Organic Chemistry 2023, 12. doi:10.1002/ajoc.202300060
  • Kotha, S.; Singh, D.; Bandi, V. Design and Synthesis of Urazole Derivatives via Ring Closing Metathesis. ChemistrySelect 2022, 7. doi:10.1002/slct.202203096
  • Haensch, V. G.; Görls, H.; Hertweck, C. A Photochemical Macrocyclization Route to Asymmetric Strained [3.2] Paracyclophanes. Chemistry (Weinheim an der Bergstrasse, Germany) 2022, 28, e202202577. doi:10.1002/chem.202202577
  • Islam, M. M.; Wang, C.-Z.; Sharma, B.; Rahman, S.; Georghiou, P. E.; Alodhayb, A.; Matsumoto, T.; Tanaka, J.; Yamato, T. Synthesis and DFT conformational analysis of trimethyl-functionalized [2.2]metacyclophanes and their Lewis-acid assisted reactions. Journal of Molecular Structure 2022, 1266, 133523. doi:10.1016/j.molstruc.2022.133523
  • Pigot, C.; Brunel, D.; Dumur, F. Indane-1,3-Dione: From Synthetic Strategies to Applications. Molecules (Basel, Switzerland) 2022, 27, 5976. doi:10.3390/molecules27185976
  • Kotha, S.; Jena, K. Ring-Rearrangement Metathetic Approach to Fused 6/5/6/5/6-Oxacyclic Ring System and Bipentalene Derivatives. Synlett 2022, 34, 850–854. doi:10.1055/a-1921-7296
Other Beilstein-Institut Open Science Activities