219 related articles for article (PubMed ID: 19788169)
1. An expeditious I2-catalyzed entry into 6H-indolo[2,3-b]quinoline system of cryptotackieine.
Parvatkar PT; Parameswaran PS; Tilve SG
J Org Chem; 2009 Nov; 74(21):8369-72. PubMed ID: 19788169
[TBL] [Abstract][Full Text] [Related]
2. Jusbetonin, the first indolo[3,2-b]quinoline alkaloid glycoside, from Justicia betonica.
Subbaraju GV; Kavitha J; Rajasekhar D; Jimenez JI
J Nat Prod; 2004 Mar; 67(3):461-2. PubMed ID: 15043432
[TBL] [Abstract][Full Text] [Related]
3. Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted 5H- and 6H-indolo[2,3-b]quinolines; structure-activity relationships of neocryptolepines and 6-methyl congeners.
Wang L; Switalska M; Mei ZW; Lu WJ; Takahara Y; Feng XW; El-Sayed Iel-T; Wietrzyk J; Inokuchi T
Bioorg Med Chem; 2012 Aug; 20(15):4820-9. PubMed ID: 22748378
[TBL] [Abstract][Full Text] [Related]
4. One-pot access to indolo[2,3-b]quinolines by electrophile-triggered cross-amination/Friedel-Crafts alkylation of indoles with 1-(2-tosylaminophenyl)ketones.
Ali S; Li YX; Anwar S; Yang F; Chen ZS; Liang YM
J Org Chem; 2012 Jan; 77(1):424-31. PubMed ID: 22136250
[TBL] [Abstract][Full Text] [Related]
5. InBr3-promoted divergent approach to polysubstituted indoles and quinolines from 2-ethynylanilines: switch from an intramolecular cyclization to an intermolecular dimerization by a type of terminal substituent group.
Sakai N; Annaka K; Fujita A; Sato A; Konakahara T
J Org Chem; 2008 Jun; 73(11):4160-5. PubMed ID: 18442294
[TBL] [Abstract][Full Text] [Related]
6. Efficient synthesis of jusbetonin, an indolo[3,2-b]quinoline glycoside, and its derivatives.
Zhang Z; Wang S; Wan S; Ren S; Li W; Jiang T
Carbohydr Res; 2009 Feb; 344(3):291-7. PubMed ID: 19110237
[TBL] [Abstract][Full Text] [Related]
7. From biomass to medicines. A simple synthesis of indolo[3,2-c]quinolines, antimalarial alkaloid isocryptolepine, and its derivatives.
Uchuskin MG; Pilipenko AS; Serdyuk OV; Trushkov IV; Butin AV
Org Biomol Chem; 2012 Sep; 10(36):7262-5. PubMed ID: 22814312
[TBL] [Abstract][Full Text] [Related]
8. A concise formal synthesis of alkaloid cryptotackiene and substituted 6H-indolo[2,3-b]quinolines.
Sundaram GS; Venkatesh C; Syam Kumar UK; Ila H; Junjappa H
J Org Chem; 2004 Aug; 69(17):5760-2. PubMed ID: 15307753
[TBL] [Abstract][Full Text] [Related]
9. An efficient iron-promoted synthesis of 6H-indolo[2,3-b]quinolines and neocryptolepine derivatives.
Yan Z; Wan C; Wan J; Wang Z
Org Biomol Chem; 2016 May; 14(19):4405-8. PubMed ID: 27117399
[TBL] [Abstract][Full Text] [Related]
10. Iodine-Mediated Intramolecular Dehydrogenative Coupling: Synthesis of N-Alkylindolo[3,2-c]- and -[2,3-c]quinoline Iodides.
Volvoikar PS; Tilve SG
Org Lett; 2016 Mar; 18(5):892-5. PubMed ID: 26866309
[TBL] [Abstract][Full Text] [Related]
11. Seco-tabersonine alkaloids from Tabernaemontana corymbosa.
Lim KH; Thomas NF; Abdullah Z; Kam TS
Phytochemistry; 2009 Feb; 70(3):424-9. PubMed ID: 19217125
[TBL] [Abstract][Full Text] [Related]
12. Pt(IV)-catalyzed hydroamination triggered cyclization: a strategy to fused pyrrolo[1,2-a]quinoxalines, indolo[1,2-a]quinoxalines, and indolo[3,2-c]quinolines.
Patil NT; Kavthe RD; Shinde VS; Sridhar B
J Org Chem; 2010 May; 75(10):3371-80. PubMed ID: 20392052
[TBL] [Abstract][Full Text] [Related]
13. An efficient synthesis of indolo[3,2-a]carbazoles via the novel acid catalyzed reaction of indoles and diaryl-1,2-diones.
Nair V; Nandialath V; Abhilash KG; Suresh E
Org Biomol Chem; 2008 May; 6(10):1738-42. PubMed ID: 18452007
[TBL] [Abstract][Full Text] [Related]
14. An alternative one-pot gold-catalyzed approach to the assembly of 11H-indolo[3,2-c]quinolines.
Abbiati G; Arcadi A; Chiarini M; Marinelli F; Pietropaolo E; Rossi E
Org Biomol Chem; 2012 Oct; 10(38):7801-8. PubMed ID: 22911041
[TBL] [Abstract][Full Text] [Related]
15. Perhydrogenation of tabersonine, ans Aspidiosperma indole alkaloid.
Lewin G; Schaeffer C; Dacquet C
J Nat Prod; 1997 Apr; 60(4):419-20. PubMed ID: 9182127
[TBL] [Abstract][Full Text] [Related]
16. Synthesis of 6-substituted 6H-indolo[2,3-b]quinolines as novel cytotoxic agents and topoisomerase II inhibitors.
Kaczmarek L; Luniewski W; Zagrodzki B; Godlewska J; Osiadacz J; Wietrzyk J; Opolski A; Peczyńska-Czoch W
Acta Pol Pharm; 2002; 59(3):199-207. PubMed ID: 12230247
[TBL] [Abstract][Full Text] [Related]
17. A flexible, convergent approach to polycyclic indole structures: formal synthesis of (+/-)-mersicarpine.
Biechy A; Zard SZ
Org Lett; 2009 Jul; 11(13):2800-3. PubMed ID: 19489601
[TBL] [Abstract][Full Text] [Related]
18. Combined directed ortho and remote metalation-cross-coupling strategies. General method for benzo[a]carbazoles and the synthesis of an unnamed indolo[2,3-a]carbazole alkaloid.
Cai X; Snieckus V
Org Lett; 2004 Jul; 6(14):2293-5. PubMed ID: 15228262
[TBL] [Abstract][Full Text] [Related]
19. The enantiospecific, stereospecific total synthesis of the ring-A oxygenated sarpagine indole alkaloids (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-N(a)-methylsarpagine, as well as the total synthesis of the alstonia bisindole alkaloid macralstonidine.
Zhao S; Liao X; Wang T; Flippen-Anderson J; Cook JM
J Org Chem; 2003 Aug; 68(16):6279-95. PubMed ID: 12895062
[TBL] [Abstract][Full Text] [Related]
20. Studies on the Claisen rearrangements in the indolo[2,3-b]quinoline system.
Voûte N; Philp D; Slawin AM; Westwood NJ
Org Biomol Chem; 2010 Jan; 8(2):442-50. PubMed ID: 20066282
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]