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Synthesis 2017; 49(20): 4606-4612
DOI: 10.1055/s-0036-1589109
DOI: 10.1055/s-0036-1589109
feature
Synthesis of Novel Iminosugar Derivatives Based on a 2-Azabicyclo[4.1.0]heptane Skeleton
Funding of this project by Spanish MINECO and Fondo Europeo de Desarrollo Regional (FEDER, grant No. CTQ2015-64624-R MINECO/FEDER) and FUSP-CEU (PC17/16) is acknowledged.Further Information
Publication History
Received: 16 June 2017
Accepted after revision: 25 August 2017
Publication Date:
12 September 2017 (online)
Abstract
Iminosugars are good starting points for the development of different kinds of drugs. Many are polyhydroxylated piperidines that behave as biomimetics of their corresponding pyranoses analogues. In the interaction with carbohydrate processing enzymes, selectivity is a crucial issue and the benefits of introducing a cyclopropane bridge in a piperidine structure is demonstrated. The synthesis of novel bicyclic piperidine-based iminosugars using a sulfur ylide cyclopropanation as the key synthetic step is described.
Key words
bicyclic compounds - piperidines - stereoselective synthesis - ylides - iminosugars - cyclopropanationSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0036-1589109.
- Supporting Information
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References
- 2a Tyrrell BE. Sayce AC. Warfield KL. Miller JL. Zitzmann N. Crit. Rev. Microbiol. 2017; 43: 521
- 2b Horne G. Wilson FX. Prog. Med. Chem. 2011; 50: 135
- 2c Nash RJ. Kato A. Yu C.-Y. Fleet GW. Future Med. Chem. 2011; 3: 1513
- 2d Wrodnigg TM. Steiner AJ. Ueberbacher BJ. Anti-Cancer Agents Med. Chem. 2008; 8: 77
- 2e Gerber-Lemaire S. Juillerat-Jeanneret L. Mini-Rev. Med. Chem. 2006; 6: 1043
- 2f Robina I. Moreno-Vargas AJ. Carmona AT. Vogel P. Curr. Drug Metab. 2004; 5: 329
- 2g Lillelund VH. Jensen HH. Liang X. Bols M. Chem. Rev. 2002; 102: 515
- 3a Compain P. Martin OR. Iminosugars: From Synthesis to Therapeutical Applications. Wiley; Chichester: 2008
- 3b Stütz AE. Iminosugars as Glycosidase Inhibitors: Nojirimycin and Beyond. Wiley-VCH; Weinheim: 1999
- 3c Butters TD. Dwek RA. Platt FM. Chem. Rev. 2000; 100: 4683
- 4a Joubert PH. Veuter CP. Joubert HF. Hillebrand I. Eur. J. Clin. Pharmacol. 1985; 28: 705
- 4b Review: Winchester BG. Tetrahedron: Asymmetry 2009; 20: 645
- 5a Yoshikuni Y. Ezure Y. Seto T. Mori K. Watanabe M. Enomoto H. Chem. Pharm. Bull. 1989; 37: 106
- 5b Markad SD. Karanjule NS. Sharma T. Sabharwal SG. Dhavele DD. Bioorg. Med. Chem. 2006; 14: 5535
- 6a Ref. 4b
- 6b Afarinkia K. Bahar A. Tetrahedron: Asymmetry 2005; 16: 1239
- 6c Pearson MS. M. Mathé-Allainmat M. Fargeas V. Lebreton J. Eur. J. Org. Chem. 2005; 2159
- 6d Ayad T. Genisson Y. Baltas M. Curr. Org. Chem. 2004; 8: 1211
- 6e Weintraub PM. Sabol JS. Kane JM. Borcherding DR. Tetrahedron 2003; 59: 2953
- 7a Niwa T. Tsuruoka T. Goi H. Kodama Y. Itoh J. Inouye S. Yamada Y. Niida T. Nobe M. Ogawa Y. J. Antibiot. (Tokyo) 1984; 37: 1579
- 7b Inouye S. Tsuroka T. Niida T. J. Antibiot. (Tokyo) 1966; 19: 288
- 8a Viuff AH. Besenbacher LM. Kamori A. Jensen MT. Kilian M. Kato A. Jensen HH. Org. Biomol. Chem. 2015; 13: 9637
- 8b Ganesan M. Salunke RV. Singh N. Ramesh NG. Org. Biomol. Chem. 2013; 11: 599
- 8c Singh A. Kim B. Lee WK. Ha H.-J. Org. Biomol. Chem. 2011; 9: 1372
- 8d Tamayo JA. Franco F. Re DL. Synlett 2010; 1323
- 8e Karjalainen OK. Passiniemi M. Koskinen AM. P. Org. Lett. 2010; 12: 1145
- 8f Bagal SK. Davies SG. Lee JA. Roberts PM. Russell AJ. Scott PM. Thomson JE. Org. Lett. 2010; 12: 136
- 8g Guaragna A. D’Errico S. D’Alonzo D. Pedatella S. Palumbo G. Org. Biomol. Chem. 2010; 8: 3307
- 8h van den Nieuwendijk AM. C. H. Ruben M. Engelsma SE. Risseeuw MD. P. van den Berg RJ. B. H. N. Boot RG. Aerts JM. Brussee J. van der Marel GA. Overkleeft HS. Org. Lett. 2010; 12: 3857
- 8i Aravind A. Sankar MG. Varghese B. Baskaran S. J. Org. Chem. 2009; 74: 2858
- 8j Palyam N. Majewski M. J. Org. Chem. 2009; 74: 4390
- 8k Rengasamy R. Curtis-Long MJ. Ryu HW. Oh KY. Park KH. Bull. Korean Chem. Soc. 2009; 30: 1531
- 8l Fu R. Du Y. Li Z.-Y. Xu W.-X. Huang P.-Q. Tetrahedron 2009; 65: 9765
- 8m Rengasamy R. Curtis-Long MJ. Seo WD. Jeong SH. Jeong I.-Y. Park KH. J. Org. Chem. 2008; 73: 2898
- 8n Kumar A. Rawal GK. Vankar YD. Tetrahedron 2008; 64: 2379
- 8o Sanap SP. Ghosh S. Jabgunde AM. Pinjari RV. Gejji SP. Singh S. Chopade BA. Dhavale DD. Org. Lett. 2007; 9: 3473
- 8p Martín R. Murruzzu C. Pericàs MA. Riera A. J. Org. Chem. 2005; 70: 3326
- 8q Takahata H. Banba Y. Ouchi H. Nemoto H. Org. Lett. 2003; 5: 2527
- 9 For a review on conformationally restricted glycoside derivatives, see: Maaliki C. Gauthier C. Massinon O. Sagar R. Vincent SP. Blériot Y. Carbohydr. Chem. 2014; 40: 418
- 10a Desire J. Shipman M. Synlett 2001; 1332
- 10b Merino P. Tejero T. Laguna M. Cerrada E. Moreno A. Lopez JA. Org. Biomol. Chem 2003; 1: 2336
- 11a Sánchez-Fernández EM. Gonçalves-Pereira R. Rísquez-Cuadro R. Plata GB. Padrón JM. García Fernández JM. Ortiz Mellet C. Carbohydr. Res. 2016; 429: 113
- 11b Li Y.-X. Shimada Y. Adachi I. Kato A. Jia Y.-M. Fleet GW. J. Xiao M. Yu C.-Y. J. Org. Chem. 2015; 80: 5151
- 11c Cipolla L. Fernandes MR. Gregori M. Airoldi C. Nicotra F. Carbohydr. Res. 2007; 342: 1813
- 12a Barbachyn MR. Ford CW. Angew. Chem. Int. Ed. 2003; 42: 2010
- 12b Schierle-Arndt K. Kolter D. Danielmeier K. Steckhan E. Eur. J. Org. Chem. 2001; 2425
- 12c Zurenko GE. Gibson JK. Shinabarger DL. Aristoff PA. Ford CW. Tarpley WG. Curr. Opin. Pharmacol. 2001; 1: 470
- 13a Niphakis MJ. Turunen BJ. Georg GI. J. Org. Chem. 2010; 75: 6793
- 13b Ege M. Wanner KT. Org. Lett. 2004; 6: 3553
- 13c Ma D. Sun H. Org. Lett. 2000; 2: 2503
- 14 Sebesta R. Pizzuti MG. Boersma AJ. Minnaard AJ. Feringa BL. Chem. Commun. 2005; 1711
- 15 López-Rodríguez A. Domínguez G. Pérez-Castells J. ChemistrySelect 2017; 2: 2565
For biological activity of iminosugars, see:
For reviews, see:
Selected recent references:
For an aziridine containing iminosugar derivative, see: