333 related articles for article (PubMed ID: 24462648)
1. Synthesis of novel 16-spiro steroids: 7-(Aryl)tetrahydro-1H-pyrrolo[1,2-c][1,3]thiazolo estrone hybrid heterocycles.
Jeyachandran V; Vivek Kumar S; Ranjith Kumar R
Steroids; 2014 Apr; 82():29-37. PubMed ID: 24462648
[TBL] [Abstract][Full Text] [Related]
2. Synthesis of novel 16-spiro steroids: spiro-7'-(aryl)tetrahydro-1H-pyrrolo[1,2-c][1,3]thiazolo-trans-androsterone hybrid heterocycles.
Kanchithalaivan S; Kumar RR; Perumal S
Steroids; 2013 Apr; 78(4):409-17. PubMed ID: 23376110
[TBL] [Abstract][Full Text] [Related]
3. A facile 1,3-dipolar cycloaddition of azomethine ylides to 2-arylidene-1,3-indanediones: synthesis of dispiro-oxindolylpyrrolothiazoles and their antimycobacterial evaluation.
Maheswari SU; Balamurugan K; Perumal S; Yogeeswari P; Sriram D
Bioorg Med Chem Lett; 2010 Dec; 20(24):7278-82. PubMed ID: 21071220
[TBL] [Abstract][Full Text] [Related]
4. A highly atom economic, chemo-, regio- and stereoselective synthesis and evaluation of spiro-pyrrolothiazoles as antitubercular agents.
Karthikeyan SV; Bala BD; Raja VP; Perumal S; Yogeeswari P; Sriram D
Bioorg Med Chem Lett; 2010 Jan; 20(1):350-3. PubMed ID: 19900810
[TBL] [Abstract][Full Text] [Related]
5. Combinatorial synthesis of functionalized spirooxindole-pyrrolidine/pyrrolizidine/pyrrolothiazole derivatives via three-component 1,3-dipolar cycloaddition reactions.
Li J; Wang J; Xu Z; Zhu S
ACS Comb Sci; 2014 Sep; 16(9):506-12. PubMed ID: 25033950
[TBL] [Abstract][Full Text] [Related]
6. An atom economic synthesis and AChE inhibitory activity of novel dispiro 7-aryltetrahydro-1H-pyrrolo[1,2-c][1,3]thiazole and 4-aryloctahydroindolizine N-methylpiperidin-4-one hybrid heterocycles.
Sivakumar S; Ranjith Kumar R; Ali MA; Choon TS
Eur J Med Chem; 2013 Jul; 65():240-8. PubMed ID: 23721952
[TBL] [Abstract][Full Text] [Related]
7. Multicomponent Dipolar Cycloaddition Strategy: Combinatorial Synthesis of Novel Spiro-Tethered Pyrazolo[3,4-b]quinoline Hybrid Heterocycles.
Sumesh RV; Muthu M; Almansour AI; Suresh Kumar R; Arumugam N; Athimoolam S; Jeya Yasmi Prabha EA; Kumar RR
ACS Comb Sci; 2016 May; 18(5):262-70. PubMed ID: 27027478
[TBL] [Abstract][Full Text] [Related]
8. A regio- and stereoselective 1,3-dipolar cycloaddition for the synthesis of novel spiro-pyrrolothiazolyloxindoles and their antitubercular evaluation.
Prasanna P; Balamurugan K; Perumal S; Yogeeswari P; Sriram D
Eur J Med Chem; 2010 Dec; 45(12):5653-61. PubMed ID: 20932607
[TBL] [Abstract][Full Text] [Related]
9. An atom economic synthesis and antitubercular evaluation of novel spiro-cyclohexanones.
Ranjith Kumar R; Perumal S; Manju SC; Bhatt P; Yogeeswari P; Sriram D
Bioorg Med Chem Lett; 2009 Jul; 19(13):3461-5. PubMed ID: 19473840
[TBL] [Abstract][Full Text] [Related]
10. One-Pot Access to a Library of Dispiro Oxindole-pyrrolidine/pyrrolothiazole-thiochromane Hybrids via Three-Component 1,3-Dipolar Cycloaddition Reactions.
Uma Rani G; Vivek Kumar S; Bharkavi C; Menéndez JC; Perumal S
ACS Comb Sci; 2016 Jun; 18(6):337-42. PubMed ID: 27073991
[TBL] [Abstract][Full Text] [Related]
11. Ultrasound-assisted sequential multicomponent strategy for the combinatorial synthesis of novel coumarin hybrids.
Kanchithalaivan S; Sumesh RV; Kumar RR
ACS Comb Sci; 2014 Oct; 16(10):566-72. PubMed ID: 25133700
[TBL] [Abstract][Full Text] [Related]
12. An expedient sequential one-pot four component synthesis of novel steroidal spiro-pyrrolidine heterocycles in ionic liquid.
Gavaskar D; Babu AR; Raghunathan R; Dharani M; Balasubramanian S
Steroids; 2016 May; 109():1-6. PubMed ID: 26930574
[TBL] [Abstract][Full Text] [Related]
13. AChE inhibitor: a regio- and stereo-selective 1,3-dipolar cycloaddition for the synthesis of novel substituted 5,6-dimethoxy spiro[5.3']-oxindole-spiro-[6.3″]-2,3-dihydro-1H-inden-1″-one-7-(substituted aryl)-tetrahydro-1H-pyrrolo[1,2-c][1,3]thiazole.
Ashraf Ali M; Ismail R; Choon TS; Kumar RS; Osman H; Arumugam N; Almansour AI; Elumalai K; Singh A
Bioorg Med Chem Lett; 2012 Jan; 22(1):508-11. PubMed ID: 22142546
[TBL] [Abstract][Full Text] [Related]
14. A One-Pot Multicomponent 1,3-Dipolar Cycloaddition Strategy: Combinatorial Synthesis of Dihydrothiophenone-Engrafted Dispiro Hybrid Heterocycles.
Anusha Rani M; Vivek Kumar S; Malathi K; Muthu M; Almansour AI; Suresh Kumar R; Ranjith Kumar R
ACS Comb Sci; 2017 May; 19(5):308-314. PubMed ID: 28371579
[TBL] [Abstract][Full Text] [Related]
15. An efficient one pot regioselective synthesis of a 3,3'-spiro-phosphonylpyrazole-oxindole framework via base mediated [1,3]-dipolar cycloaddition reaction of the Bestmann-Ohira reagent with methyleneindolinones.
Shelke AM; Suryavanshi G
Org Biomol Chem; 2015 Aug; 13(32):8669-75. PubMed ID: 26177837
[TBL] [Abstract][Full Text] [Related]
16. Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction.
Haddad S; Boudriga S; Porzio F; Soldera A; Askri M; Knorr M; Rousselin Y; Kubicki MM; Golz C; Strohmann C
J Org Chem; 2015 Sep; 80(18):9064-75. PubMed ID: 26291879
[TBL] [Abstract][Full Text] [Related]
17. Stereoselective synthesis of spiro and condensed pyrazolines of steroidal alpha,beta-unsaturated ketones and nitrilimines by 1,3-dipolar cycloaddition.
Mernyák E; Kozma E; Hetényi A; Márk L; Schneider G; Wölfling J
Steroids; 2009 Jun; 74(6):520-5. PubMed ID: 19428440
[TBL] [Abstract][Full Text] [Related]
18. Synthesis of pyrrolo(spiro-[2.3']-oxindole)-spiro-[4.3"]-oxindole via 1,3-dipolar cycloaddition of azomethine ylides with 3-acetonylideneoxindole.
Xiao JA; Zhang HG; Liang S; Ren JW; Yang H; Chen XQ
J Org Chem; 2013 Nov; 78(22):11577-83. PubMed ID: 24111532
[TBL] [Abstract][Full Text] [Related]
19. A facile synthesis and antimycobacterial evaluation of novel spiro-pyrido-pyrrolizines and pyrrolidines.
Ranjith Kumar R; Perumal S; Senthilkumar P; Yogeeswari P; Sriram D
Eur J Med Chem; 2009 Sep; 44(9):3821-9. PubMed ID: 19524332
[TBL] [Abstract][Full Text] [Related]
20. Synthesis and QSAR study of novel cytotoxic spiro[3H-indole-3,2'(1'H)-pyrrolo[3,4-c]pyrrole]-2,3',5'(1H,2'aH,4'H)-triones.
Girgis AS; Stawinski J; Ismail NS; Farag H
Eur J Med Chem; 2012 Jan; 47(1):312-22. PubMed ID: 22119131
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]