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405 related items for PubMed ID: 17927252
1. Synthesis of 7-azabicyclo[2.2.1]heptane and 2-oxa-4-azabicyclo[3.3.1]non-3-ene derivatives by base-promoted heterocyclization of alkyl N-(cis(trans)-3,trans(cis)-4-dibromocyclohex-1-yl)carbamates and N-(cis(trans)-3,trans(cis)-4-dibromocyclohex-1-yl)-2,2,2-trifluoroacetamides. Gómez-Sanchez E, Soriano E, Marco-Contelles J. J Org Chem; 2007 Nov 09; 72(23):8656-70. PubMed ID: 17927252 [Abstract] [Full Text] [Related]
2. Synthesis of heterocyclic analogues of epibatidine via 7-azabicyclo[2.2.1]hept-2-yl radical intermediates. 1. Intermolecular reactions. Gómez-Sánchez E, Soriano E, Marco-Contelles J. J Org Chem; 2008 Sep 05; 73(17):6784-92. PubMed ID: 18656981 [Abstract] [Full Text] [Related]
3. Mechanistic analysis of intramolecular free radical reactions toward synthesis of 7-azabicyclo[2.2.1]heptane derivatives. Soriano E, Marco-Contelles J. J Org Chem; 2009 Jun 05; 74(11):4061-7. PubMed ID: 19402620 [Abstract] [Full Text] [Related]
4. Microwave-assisted synthesis of novel (5-nitropyridin-2-yl)alkyl and (5-nitropyridin-3-yl)alkyl carbamates. Henry C, Haupt A, Turner SC. J Org Chem; 2009 Mar 06; 74(5):1932-8. PubMed ID: 19175330 [Abstract] [Full Text] [Related]
5. 7-substituted 2-azabicyclo[2.2.1]heptanes as key intermediates for the synthesis of novel epibatidine analogues; synthesis of syn-and anti-isoepiboxidine. Malpass JR, White R. J Org Chem; 2004 Aug 06; 69(16):5328-34. PubMed ID: 15287778 [Abstract] [Full Text] [Related]
6. Aza-Prins-pinacol approach to 7-azabicyclo[2.2.1]heptanes: syntheses of (+/-)-epibatidine and (+/-)-epiboxidine. Armstrong A, Bhonoah Y, Shanahan SE. J Org Chem; 2007 Oct 12; 72(21):8019-24. PubMed ID: 17867705 [Abstract] [Full Text] [Related]
7. Asymmetric synthesis of 3,4-diaminocyclohexanol and endo-7-azabicyclo[2.2.1]heptan-2-amine. Savoia D, Grilli S, Gualandi A. Org Lett; 2010 Nov 05; 12(21):4964-7. PubMed ID: 20932021 [Abstract] [Full Text] [Related]
8. A novel intramolecular Ugi reaction with 7-azabicyclo[2.2.1]heptane derivatives followed by post-condensation acylations: a new entry to azanorbornyl peptidomimetics. Basso A, Banfi L, Guanti G, Riva R. Org Biomol Chem; 2009 Jan 21; 7(2):253-8. PubMed ID: 19109669 [Abstract] [Full Text] [Related]
9. Intramolecular hydrogen abstraction reaction promoted by N-radicals in carbohydrates. Synthesis of chiral 7-oxa-2-azabicyclo[2.2.1]heptane and 8-oxa-6-azabicyclo[3.2.1]octane ring systems. Francisco CG, Herrera AJ, Suárez E. J Org Chem; 2003 Feb 07; 68(3):1012-7. PubMed ID: 12558429 [Abstract] [Full Text] [Related]
10. C(8) substituted 1-azabicyclo[3.3.1]non-3-enes and C(8) substituted 1-azabicyclo[3.3.1]nonan-4-ones: novel muscarinic receptor antagonists. Kim MG, Bodor ET, Wang C, Harden TK, Kohn H. J Med Chem; 2003 May 22; 46(11):2216-26. PubMed ID: 12747793 [Abstract] [Full Text] [Related]
11. Synthesis of all four stereoisomers of 3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-2-carboxylic acid. Bakonyi B, Furegati M, Kramer C, La Vecchia L, Ossola F. J Org Chem; 2013 Sep 20; 78(18):9328-39. PubMed ID: 23957679 [Abstract] [Full Text] [Related]
12. Synthesis of enantiomerically pure 1,2-diamine derivatives of 7-azabicyclo[2.2.1]heptane. New leads as glycosidase inhibitors and rigid scaffolds for the preparation of peptide analogues. Moreno-Vargas AJ, Schütz C, Scopelliti R, Vogel P. J Org Chem; 2003 Jul 11; 68(14):5632-40. PubMed ID: 12839456 [Abstract] [Full Text] [Related]
13. Synthesis of 3-azabicyclo[3.1.0]hexane derivatives via palladium-catalyzed cyclopropanation of maleimides with N-tosylhydrazones: practical and facile access to CP-866,087. Chen P, Zhu C, Zhu R, Lin Z, Wu W, Jiang H. Org Biomol Chem; 2017 Feb 01; 15(5):1228-1235. PubMed ID: 28094400 [Abstract] [Full Text] [Related]
14. An unexpected formation of the novel 7-oxa-2-azabicyclo[2.2.1]hept-5-ene skeleton during the reaction of furfurylamine with maleimides and their bioprospection using a zebrafish embryo model. Puerto Galvis CE, Kouznetsov VV. Org Biomol Chem; 2013 Jan 21; 11(3):407-11. PubMed ID: 23192531 [Abstract] [Full Text] [Related]
16. Synthesis of n-heteroaryl-7-azabicyclo[2.2.1]heptane derivatives via palladium-bisimidazol-2-ylidene complex catalyzed amination reactions. Cheng J, Trudell ML. Org Lett; 2001 May 03; 3(9):1371-4. PubMed ID: 11348237 [Abstract] [Full Text] [Related]
17. Synthesis of N-substituted 9-azabicyclo[3.3.1]nonan-3alpha-yl carbamate analogs as sigma2 receptor ligands. Vangveravong S, Xu J, Zeng C, Mach RH. Bioorg Med Chem; 2006 Oct 15; 14(20):6988-97. PubMed ID: 16837201 [Abstract] [Full Text] [Related]
18. Derivatives of (-)-7-methyl-2-(5-(pyridinyl)pyridin-3-yl)-7-azabicyclo[2.2.1]heptane are potential ligands for positron emission tomography imaging of extrathalamic nicotinic acetylcholine receptors. Gao Y, Horti AG, Kuwabara H, Ravert HT, Hilton J, Holt DP, Kumar A, Alexander M, Endres CJ, Wong DF, Dannals RF. J Med Chem; 2007 Aug 09; 50(16):3814-24. PubMed ID: 17629263 [Abstract] [Full Text] [Related]
19. Structure revision and syntheses of epohelmins A and B. Snider BB, Gao X. Org Lett; 2005 Sep 29; 7(20):4419-22. PubMed ID: 16178548 [Abstract] [Full Text] [Related]
20. Approaches to syn-7-substituted 2-azanorbornanes as potential nicotinic agonists; synthesis of syn- and anti-isoepibatidine. Malpass JR, Handa S, White R. Org Lett; 2005 Jun 23; 7(13):2759-62. PubMed ID: 15957940 [Abstract] [Full Text] [Related] Page: [Next] [New Search]