Supporting Information
Supporting Information File 1: Full experimental details, analytical data and crystallographic information. | ||
Format: PDF | Size: 1.5 MB | Download |
Cite the Following Article
One-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: Facile access to chiral 10-heteroazatriquinanes
Ping-An Wang, Sheng-Yong Zhang and Henri B. Kagan
Beilstein J. Org. Chem. 2013, 9, 265–269.
https://doi.org/10.3762/bjoc.9.32
How to Cite
Wang, P.-A.; Zhang, S.-Y.; Kagan, H. B. Beilstein J. Org. Chem. 2013, 9, 265–269. doi:10.3762/bjoc.9.32
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
- Masusai, C.; Soorukram, D.; Kuhakarn, C.; Reutrakul, V.; Pohmakotr, M. Stereoselective Synthesis of gem-Difluoromethylenated Linear Azatriquinanes. European Journal of Organic Chemistry 2018, 2018, 160–169. doi:10.1002/ejoc.201701415
- Iovan, D. A.; Wilding, M. J. T.; Baek, Y.; Hennessy, E. T.; Betley, T. A. Diastereoselective C−H Bond Amination for Disubstituted Pyrrolidines. Angewandte Chemie 2017, 129, 15805–15808. doi:10.1002/ange.201708519
- Iovan, D. A.; Wilding, M. J. T.; Baek, Y.; Hennessy, E. T.; Betley, T. A. Diastereoselective C-H Bond Amination for Disubstituted Pyrrolidines. Angewandte Chemie (International ed. in English) 2017, 56, 15599–15602. doi:10.1002/anie.201708519
- Jia, Y.; Li, X.-Y.; Wang, P.-A.; Wen, A. Facile access to unnatural dipeptide-alcohols based on cis-2,5-disubstituted pyrrolidines. Molecules (Basel, Switzerland) 2015, 20, 2922–2930. doi:10.3390/molecules20022922
- Amara, Z.; Drège, E.; Troufflard, C.; Retailleau, P.; Huu‐Dau, M. T.; Joseph, D. Switchable Stereocontrolled Divergent Synthesis Induced by aza‐Michael Addition of Deactivated Primary Amines under Acid Catalysis. Chemistry (Weinheim an der Bergstrasse, Germany) 2014, 20, 15840–15848. doi:10.1002/chem.201404589
- Butnariu, M. Physiological Accessibility of the Substances with Action Pharmacological. Journal of Bioequivalence & Bioavailability 2014, 2014.