922 related articles for article (PubMed ID: 24730692)
1. Catalytic enantioselective 1,3-dipolar cycloadditions of azomethine ylides for biology-oriented synthesis.
Narayan R; Potowski M; Jia ZJ; Antonchick AP; Waldmann H
Acc Chem Res; 2014 Apr; 47(4):1296-310. PubMed ID: 24730692
[TBL] [Abstract][Full Text] [Related]
2. Catalytic Asymmetric Reactions with
Wei L; Chang X; Wang CJ
Acc Chem Res; 2020 May; 53(5):1084-1100. PubMed ID: 32320206
[TBL] [Abstract][Full Text] [Related]
3. 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides with Carbonyl Dipolarophiles Yielding Oxazolidine Derivatives.
Meyer AG; Ryan JH
Molecules; 2016 Jul; 21(8):. PubMed ID: 27455230
[TBL] [Abstract][Full Text] [Related]
4. exo-Selective construction of spiro-[butyrolactone-pyrrolidine] via 1,3-dipolar cycloaddition of azomethine ylides with α-methylene-γ-butyrolactone catalyzed by Cu(I)/DTBM-BIPHEP.
Li QH; Liu TL; Wei L; Zhou X; Tao HY; Wang CJ
Chem Commun (Camb); 2013 Oct; 49(83):9642-4. PubMed ID: 24022250
[TBL] [Abstract][Full Text] [Related]
5. Synthesis of benzosuberone-tethered spirooxindoles: 1-3-dipolar cycloaddition of azomethine ylides and arylidene benzosuberones.
Kumar SV; Rani GU; Divyalakshmi M; Bhuvanesh N; Muthusubramanian S; Perumal S
Mol Divers; 2019 Aug; 23(3):669-680. PubMed ID: 30535898
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Catalytic enantioselective intramolecular 1,3-dipolar cycloaddition of azomethine ylides with fluorinated dipolarophiles.
Cristóbal C; Gaviña D; Alonso I; Ribagorda M; Carretero JC; Del Pozo C; Adrio J
Chem Commun (Camb); 2022 Jul; 58(56):7805-7808. PubMed ID: 35735739
[TBL] [Abstract][Full Text] [Related]
8. 1,3-Dipolar cycloaddition reactions of azomethine ylides with a cellulose-derived chiral enone. A novel route for organocatalysts development.
Sarotti AM; Spanevello RA; Suárez AG; Echeverría GA; Piro OE
Org Lett; 2012 May; 14(10):2556-9. PubMed ID: 22545814
[TBL] [Abstract][Full Text] [Related]
9. Catalytic asymmetric construction of quaternary α-amino acid containing pyrrolidines through 1,3-dipolar cycloaddition of azomethine ylides to α-aminoacrylates.
Wang Z; Luo S; Zhang S; Yang WL; Liu YZ; Li H; Luo X; Deng WP
Chemistry; 2013 May; 19(21):6739-45. PubMed ID: 23553867
[TBL] [Abstract][Full Text] [Related]
10. Highly enantioselective asymmetric 1,3-dipolar cycloaddition of azomethine ylide catalyzed by a copper(I)/ClickFerrophos complex.
Fukuzawa S; Oki H
Org Lett; 2008 May; 10(9):1747-50. PubMed ID: 18373347
[TBL] [Abstract][Full Text] [Related]
11. Highly enantioselective catalytic 1,3-dipolar cycloaddition involving 2,3-allenoate dipolarophiles.
Yu J; He L; Chen XH; Song J; Chen WJ; Gong LZ
Org Lett; 2009 Nov; 11(21):4946-9. PubMed ID: 19813752
[TBL] [Abstract][Full Text] [Related]
12. Catalytic asymmetric 1,3-dipolar cycloaddition of N-unprotected 2-oxoindolin-3-ylidene derivatives and azomethine ylides for the construction of spirooxindole-pyrrolidines.
Liu TL; Xue ZY; Tao HY; Wang CJ
Org Biomol Chem; 2011 Mar; 9(6):1980-6. PubMed ID: 21270976
[TBL] [Abstract][Full Text] [Related]
13. A Facile One-Pot Construction of Succinimide-Fused Spiro[Pyrrolidine-2,3'-Oxindoles] via 1,3-Dipolar Cycloaddition Involving 3-Amino Oxindoles and Maleimides.
Jin L; Liang F
Molecules; 2018 Mar; 23(3):. PubMed ID: 29510590
[TBL] [Abstract][Full Text] [Related]
14. Binaphthol-derived bisphosphoric acids serve as efficient organocatalysts for highly enantioselective 1,3-dipolar cycloaddition of azomethine ylides to electron-deficient olefins.
He L; Chen XH; Wang DN; Luo SW; Zhang WQ; Yu J; Ren L; Gong LZ
J Am Chem Soc; 2011 Aug; 133(34):13504-18. PubMed ID: 21780781
[TBL] [Abstract][Full Text] [Related]
15. Enantioselective synthesis of 4-aminopyrrolidine-2,4-dicarboxylate derivatives via Ag-catalyzed cycloaddition of azomethine ylides with alkylidene azlactones.
González-Esguevillas M; Adrio J; Carretero JC
Chem Commun (Camb); 2013 May; 49(41):4649-51. PubMed ID: 23579920
[TBL] [Abstract][Full Text] [Related]
16. Ligand-Controlled Diastereoselective 1,3-Dipolar Cycloadditions of Azomethine Ylides with Methacrylonitrile.
Walton MC; Yang YF; Hong X; Houk KN; Overman LE
Org Lett; 2015 Dec; 17(24):6166-9. PubMed ID: 26605985
[TBL] [Abstract][Full Text] [Related]
17. Highly enantioselective intramolecular 1,3-dipolar cycloaddition: a route to piperidino-pyrrolizidines.
Vidadala SR; Golz C; Strohmann C; Daniliuc CG; Waldmann H
Angew Chem Int Ed Engl; 2015 Jan; 54(2):651-5. PubMed ID: 25393926
[TBL] [Abstract][Full Text] [Related]
18. Asymmetic organocatalytic 1,3-dipolar cycloaddition of azomethine ylide to methyl 2-(2-nitrophenyl)acrylate for the synthesis of diastereoisomers of spirotryprostatin A.
Cheng MN; Wang H; Gong LZ
Org Lett; 2011 May; 13(9):2418-21. PubMed ID: 21486026
[TBL] [Abstract][Full Text] [Related]
19. Stereoselective construction of a 5-aza-spiro[2,4]heptane motif via catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides and ethyl cyclopropylidene acetate.
Liu TL; He ZL; Tao HY; Cai YP; Wang CJ
Chem Commun (Camb); 2011 Mar; 47(9):2616-8. PubMed ID: 21234474
[TBL] [Abstract][Full Text] [Related]
20. The [3 + 3]-cycloaddition alternative for heterocycle syntheses: catalytically generated metalloenolcarbenes as dipolar adducts.
Xu X; Doyle MP
Acc Chem Res; 2014 Apr; 47(4):1396-405. PubMed ID: 24650430
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]