These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
110 related articles for article (PubMed ID: 22976923)
1. Enantioselective synthesis of tetrahydrocarbazoles through a Michael addition/Ciamician-Plancher rearrangement sequence: asymmetric synthesis of a potent constrained analogue of MS-245. Loh CC; Raabe G; Enders D Chemistry; 2012 Oct; 18(42):13250-4. PubMed ID: 22976923 [No Abstract] [Full Text] [Related]
2. A silver-promoted auto-tandem catalysis for the synthesis of multiply substituted tetrahydrocarbazoles. Wang MZ; Zhou CY; Che CM Chem Commun (Camb); 2011 Jan; 47(4):1312-4. PubMed ID: 21120247 [TBL] [Abstract][Full Text] [Related]
3. Asymmetric Diels-Alder reaction of 2-methyl-3-indolylmethanols via in situ generation of o-quinodimethanes. Xiao YC; Zhou QQ; Dong L; Liu TY; Chen YC Org Lett; 2012 Dec; 14(23):5940-3. PubMed ID: 23186032 [TBL] [Abstract][Full Text] [Related]
4. Interaction of chiral MS-245 analogs at h5-HT6 receptors. Abate C; Kolanos R; Dukat M; Setola V; Roth BL; Glennon RA Bioorg Med Chem Lett; 2005 Aug; 15(15):3510-3. PubMed ID: 15990303 [TBL] [Abstract][Full Text] [Related]
6. One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles. Liu QJ; Yan WG; Wang L; Zhang XP; Tang Y Org Lett; 2015 Aug; 17(16):4014-7. PubMed ID: 26252859 [TBL] [Abstract][Full Text] [Related]
7. The asymmetric Cu(II)-indolinylmethanol complex catalyzed Diels-Alder reaction of 2-vinylindoles with β,γ-unsaturated α-ketoesters: an efficient route to functionalized tetrahydrocarbazoles. Ouyang B; Yu T; Luo R; Lu G Org Biomol Chem; 2014 Jun; 12(24):4172-6. PubMed ID: 24828971 [TBL] [Abstract][Full Text] [Related]
8. Mapping the melatonin receptor. 5. Melatonin agonists and antagonists derived from tetrahydrocyclopent[b]indoles, tetrahydrocarbazoles and hexahydrocyclohept[b]indoles. Davies DJ; Garratt PJ; Tocher DA; Vonhoff S; Davies J; Teh MT; Sugden D J Med Chem; 1998 Feb; 41(4):451-67. PubMed ID: 9484496 [TBL] [Abstract][Full Text] [Related]
9. A regiospecific synthesis of a series of 1-sulfonyl azepinoindoles as potent 5-HT6 ligands. Liu KG; Lo JR; Comery TA; Zhang GM; Zhang JY; Kowal DM; Smith DL; Di L; Kerns EH; Schechter LE; Robichaud AJ Bioorg Med Chem Lett; 2008 Jul; 18(14):3929-31. PubMed ID: 18583130 [TBL] [Abstract][Full Text] [Related]
10. Enantioselective construction of pyrroloindolines via chiral phosphoric acid catalyzed cascade Michael addition-cyclization of tryptamines. Cai Q; Liu C; Liang XW; You SL Org Lett; 2012 Sep; 14(17):4588-90. PubMed ID: 22928846 [TBL] [Abstract][Full Text] [Related]
15. Enantioselective intermolecular formal [3 + 3] cycloaddition of 2,3-disubstituted indoles with acrolein. Huang J; Zhao L; Liu Y; Cao W; Wu X Org Lett; 2013 Sep; 15(17):4338-41. PubMed ID: 23947569 [TBL] [Abstract][Full Text] [Related]
16. N1-(Benzenesulfonyl)tryptamines as novel 5-HT6 antagonists. Tsai Y; Dukat M; Slassi A; MacLean N; Demchyshyn L; Savage JE; Roth BL; Hufesein S; Lee M; Glennon RA Bioorg Med Chem Lett; 2000 Oct; 10(20):2295-9. PubMed ID: 11055342 [TBL] [Abstract][Full Text] [Related]
17. Enantioselective Friedel-Crafts alkylation of indoles with alkylidene malonates catalyzed by N,N'-dioxide-scandium(III) complexes: asymmetric synthesis of beta-carbolines. Liu Y; Shang D; Zhou X; Liu X; Feng X Chemistry; 2009; 15(9):2055-8. PubMed ID: 19177478 [TBL] [Abstract][Full Text] [Related]
18. An enantioselective approach to highly substituted tetrahydrocarbazoles through hydrogen bonding-catalyzed cascade reactions. Wang XF; Chen JR; Cao YJ; Cheng HG; Xiao WJ Org Lett; 2010 Mar; 12(5):1140-3. PubMed ID: 20146508 [TBL] [Abstract][Full Text] [Related]
19. A one-pot synthesis of 7-phenylindolo[3,2-a]carbazoles from indoles and β-nitrostyrenes, via an unprecedented reaction sequence. Dupeyre G; Lemoine P; Ainseba N; Michel S; Cachet X Org Biomol Chem; 2011 Oct; 9(22):7780-90. PubMed ID: 21975909 [TBL] [Abstract][Full Text] [Related]
20. 3-(Arylsulfonyl)-1-(azacyclyl)-1H-indoles are 5-HT(6) receptor modulators. Bernotas RC; Antane S; Shenoy R; Le VD; Chen P; Harrison BL; Robichaud AJ; Zhang GM; Smith D; Schechter LE Bioorg Med Chem Lett; 2010 Mar; 20(5):1657-60. PubMed ID: 20138763 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]