151 related articles for article (PubMed ID: 22316241)
1. Synthesis of polysubstituted, functionalized quinolines through a metal-free domino process involving a C4–C3 functional group rearrangement.
Ribelles P; Ramos MT; Menéndez JC
Org Lett; 2012 Mar; 14(6):1402-4. PubMed ID: 22316241
[TBL] [Abstract][Full Text] [Related]
2. FeCl3-mediated synthesis of polysubstituted tetrahydroquinolines via domino Mannich/Friedel-Crafts reactions of aldehydes and amines.
Yang YF; Shu XZ; Wei HL; Luo JY; Ali S; Liu XY; Liang YM
Org Biomol Chem; 2011 Jul; 9(14):5028-33. PubMed ID: 21643590
[TBL] [Abstract][Full Text] [Related]
3. Highly enantioselective synthesis of polysubstituted tetrahydroquinolines via organocatalytic Michael/Aza-Henry tandem reactions.
Jia ZX; Luo YC; Xu PF
Org Lett; 2011 Mar; 13(5):832-5. PubMed ID: 21288007
[TBL] [Abstract][Full Text] [Related]
4. The first aza Diels-Alder reaction involving an alpha,beta-unsaturated hydrazone as the dienophile: stereoselective synthesis of C-4 functionalized 1,2,3,4-tetrahydroquinolines containing a quaternary stereocenter.
Sridharan V; Perumal PT; Avendaño C; Menéndez JC
Org Biomol Chem; 2007 May; 5(9):1351-3. PubMed ID: 17464403
[TBL] [Abstract][Full Text] [Related]
5. Efficient entry into 2-substituted tetrahydroquinoline systems through alkylative ring expansion: stereoselective formal synthesis of (+/-)-martinellic acid.
Ueda M; Kawai S; Hayashi M; Naito T; Miyata O
J Org Chem; 2010 Feb; 75(3):914-21. PubMed ID: 20063853
[TBL] [Abstract][Full Text] [Related]
6. Efficient synthesis of 5H-cyclopenta[c]quinoline derivatives via palladium-catalyzed domino reactions of o-alkynylhalobenzene with amine.
Luo Y; Pan X; Wu J
Org Lett; 2011 Mar; 13(5):1150-3. PubMed ID: 21306155
[TBL] [Abstract][Full Text] [Related]
7. Microwave-assisted domino access to C2-chain functionalized furans from tertiary propargyl vinyl ethers.
Tejedor D; Cotos L; García-Tellado F
Org Lett; 2011 Aug; 13(16):4422-5. PubMed ID: 21780753
[TBL] [Abstract][Full Text] [Related]
8. Electrophile-driven regioselective synthesis of functionalized quinolines.
Ali S; Zhu HT; Xia XF; Ji KG; Yang YF; Song XR; Liang YM
Org Lett; 2011 May; 13(10):2598-601. PubMed ID: 21491872
[TBL] [Abstract][Full Text] [Related]
9. A catalytic asymmetric ring-expansion reaction of isatins and α-alkyl-α-diazoesters: highly efficient synthesis of functionalized 2-quinolone derivatives.
Li W; Liu X; Hao X; Cai Y; Lin L; Feng X
Angew Chem Int Ed Engl; 2012 Aug; 51(34):8644-7. PubMed ID: 22821752
[TBL] [Abstract][Full Text] [Related]
10. Highly enantioselective assembly of functionalized tetrahydroquinolines with creation of an all-carbon quaternary center.
Tan HR; Ng HF; Chang J; Wang J
Chemistry; 2012 Mar; 18(13):3865-70. PubMed ID: 22378143
[No Abstract] [Full Text] [Related]
11. Direct enantioselective access to 4-substituted tetrahydroquinolines by catalytic asymmetric transfer hydrogenation of quinolines.
Rueping M; Theissmann T; Stoeckel M; Antonchick AP
Org Biomol Chem; 2011 Oct; 9(19):6844-50. PubMed ID: 21837348
[TBL] [Abstract][Full Text] [Related]
12. Alkyltriflate-triggered annulation of arylisothiocyanates and alkynes leading to multiply substituted quinolines through domino electrophilic activation.
Zhao P; Yan X; Yin H; Xi C
Org Lett; 2014 Feb; 16(4):1120-3. PubMed ID: 24517410
[TBL] [Abstract][Full Text] [Related]
13. Organocatalytic aza-Michael-Michael cascade reactions: a flexible approach to 2,3,4-trisubstituted tetrahydroquinolines.
Jia ZX; Luo YC; Wang Y; Chen L; Xu PF; Wang B
Chemistry; 2012 Oct; 18(41):12958-61. PubMed ID: 23002000
[TBL] [Abstract][Full Text] [Related]
14. Enantioselective organocatalytic C-H bond functionalization via tandem 1,5-hydride transfer/ring closure: asymmetric synthesis of tetrahydroquinolines.
Kang YK; Kim SM; Kim DY
J Am Chem Soc; 2010 Sep; 132(34):11847-9. PubMed ID: 20701277
[TBL] [Abstract][Full Text] [Related]
15. A new rapid multicomponent domino reaction for the formation of functionalized benzo[h]pyrazolo[3,4-b]quinolines.
Jiang B; Zhang G; Ma N; Shi F; Tu SJ; Kaur P; Li G
Org Biomol Chem; 2011 May; 9(10):3834-8. PubMed ID: 21445382
[TBL] [Abstract][Full Text] [Related]
16. An organocatalytic cascade approach toward polysubstituted quinolines and chiral 1,4-dihydroquinolines-unanticipated effect of N-protecting groups.
Zhang X; Song X; Li H; Zhang S; Chen X; Yu X; Wang W
Angew Chem Int Ed Engl; 2012 Jul; 51(29):7282-6. PubMed ID: 22696453
[TBL] [Abstract][Full Text] [Related]
17. Multicomponent reactions with dihydroazines: efficient synthesis of a diverse set of pyrido-fused tetrahydroquinolines.
Carranco I; Díaz JL; Jiménez O; Vendrell M; Albericio F; Royo M; Lavilla R
J Comb Chem; 2005; 7(1):33-41. PubMed ID: 15638476
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Regioselective, Molecular Iodine-Mediated C3 Iodination of Quinolines.
Sun K; Lv Y; Wang J; Sun J; Liu L; Jia M; Liu X; Li Z; Wang X
Org Lett; 2015 Sep; 17(18):4408-11. PubMed ID: 26235562
[TBL] [Abstract][Full Text] [Related]
20. Mannich Bases as Enone Precursors for Water-Mediated Efficient Synthesis of 2,3,6-Trisubstituted Pyridines and 5,6,7,8-Tetrahydroquinolines.
Hanashalshahaby EH; Unaleroglu C
ACS Comb Sci; 2015 Jun; 17(6):374-80. PubMed ID: 25961906
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
