162 related articles for article (PubMed ID: 30864430)
1. "On Water" Direct Organocatalytic Cyanoarylmethylation of Isatins for the Diastereoselective Synthesis of 3-Hydroxy-3-cyanomethyl Oxindoles.
Zhang Y; Luo L; Ge J; Yan SQ; Peng YX; Liu YR; Liu JX; Liu C; Ma T; Luo HQ
J Org Chem; 2019 Apr; 84(7):4000-4008. PubMed ID: 30864430
[TBL] [Abstract][Full Text] [Related]
2. Catalytic Enantioselective Ynamide Additions to Isatins: Concise Access to Oxindole Alkaloids.
Moskowitz M; Wolf C
Angew Chem Int Ed Engl; 2019 Mar; 58(11):3402-3406. PubMed ID: 30695127
[TBL] [Abstract][Full Text] [Related]
3. Dual organocatalytic activation of isatins and formaldehyde tert-butyl hydrazone: asymmetric synthesis of functionalized 3-hydroxy-2-oxindoles.
Monge D; Crespo-Peña AM; Martín-Zamora E; Álvarez E; Fernández R; Lassaletta JM
Chemistry; 2013 Jun; 19(26):8421-5. PubMed ID: 23670976
[TBL] [Abstract][Full Text] [Related]
4. Bismuth(iii)-catalyzed regioselective alkylation of tetrahydroquinolines and indolines towards the synthesis of bioactive core-biaryl oxindoles and CYP19 inhibitors.
Prusty N; Kinthada LK; Meena R; Chebolu R; Ravikumar PC
Org Biomol Chem; 2021 Jan; 19(4):891-905. PubMed ID: 33410845
[TBL] [Abstract][Full Text] [Related]
5. Enantioselective construction of 3-hydroxy oxindoles via decarboxylative addition of β-ketoacids to isatins.
Zhong F; Yao W; Dou X; Lu Y
Org Lett; 2012 Aug; 14(15):4018-21. PubMed ID: 22830448
[TBL] [Abstract][Full Text] [Related]
6. Enantioselective synthesis of 3-hydroxy oxindoles by ytterbium-catalysed decarboxylative addition of β-ketoacids to isatins.
Duan Z; Han J; Qian P; Zhang Z; Wang Y; Pan Y
Org Biomol Chem; 2013 Oct; 11(38):6456-9. PubMed ID: 23979548
[TBL] [Abstract][Full Text] [Related]
7. Me-BIPAM for the synthesis of optically active 3-aryl-3-hydroxy-2-oxindoles by ruthenium-catalyzed addition of arylboronic acids to isatins.
Yamamoto Y; Yohda M; Shirai T; Ito H; Miyaura N
Chem Asian J; 2012 Oct; 7(10):2446-9. PubMed ID: 22807409
[TBL] [Abstract][Full Text] [Related]
8. Organocatalytic asymmetric Friedel-Crafts reaction of sesamol with isatins: access to biologically relevant 3-aryl-3-hydroxy-2-oxindoles.
Kumar A; Kaur J; Chauhan P; Chimni SS
Chem Asian J; 2014 May; 9(5):1305-10. PubMed ID: 24591414
[TBL] [Abstract][Full Text] [Related]
9. Facile creation of 3-substituted-3-hydroxy-2-oxindoles by arginine-catalyzed aldol reactions of α,β-unsaturated ketones with isatins.
Yan T; Wang X; Sun H; Liu J; Xie Y
Molecules; 2013 Nov; 18(12):14505-18. PubMed ID: 24287987
[TBL] [Abstract][Full Text] [Related]
10. Enantioselective Morita-Baylis-Hillman reaction of isatins with acrylates: facile creation of 3-hydroxy-2-oxindoles.
Zhong F; Chen GY; Lu Y
Org Lett; 2011 Jan; 13(1):82-5. PubMed ID: 21138329
[TBL] [Abstract][Full Text] [Related]
11. Asymmetric Construction of Bispiro[oxindole-pyrrolidine-rhodanine]s via Squaramide-Catalyzed Domino Michael/Mannich [3 + 2] Cycloaddition of Rhodanine Derivatives with N-(2,2,2-Trifluoroethyl)isatin Ketimines.
Song YX; Du DM
J Org Chem; 2018 Aug; 83(16):9278-9290. PubMed ID: 29956933
[TBL] [Abstract][Full Text] [Related]
12. Synthesis of Spirooxindoles via the tert-Amino Effect.
Ramakumar K; Maji T; Partridge JJ; Tunge JA
Org Lett; 2017 Aug; 19(15):4014-4017. PubMed ID: 28737400
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of spiro-tetrahydrothiopyran-oxindoles by Michael-aldol cascade reactions: discovery of potential P53-MDM2 inhibitors with good antitumor activity.
Wang S; Chen S; Guo Z; He S; Zhang F; Liu X; Chen W; Zhang S; Sheng C
Org Biomol Chem; 2018 Jan; 16(4):625-634. PubMed ID: 29302672
[TBL] [Abstract][Full Text] [Related]
14. Aqueous Morita-Baylis-Hillman reaction of unprotected isatins with cyclic enones.
Gomes JC; Sirvent J; Moyano A; Rodrigues MT; Coelho F
Org Lett; 2013 Nov; 15(22):5838-41. PubMed ID: 24188034
[TBL] [Abstract][Full Text] [Related]
15. Diastereoselective Addition of PhSCF
Keereewan S; Kuhakarn C; Leowanawat P; Saithong S; Reutrakul V; Soorukram D
J Org Chem; 2022 Dec; 87(23):15963-15985. PubMed ID: 36366856
[TBL] [Abstract][Full Text] [Related]
16. Rhodium(II) catalyzed diastereoselective reactions of diazoacetamides with isatins: an efficient approach to 3-hydroxy-3,3'-bioxindoles.
Li M; Zan L; Prajapati D; Hu W
Org Biomol Chem; 2012 Nov; 10(44):8808-13. PubMed ID: 23042091
[TBL] [Abstract][Full Text] [Related]
17. Copper-catalyzed asymmetric addition of arylboronates to isatins: a catalytic cycle involving alkoxocopper intermediates.
Shintani R; Takatsu K; Hayashi T
Chem Commun (Camb); 2010 Sep; 46(36):6822-4. PubMed ID: 20725672
[TBL] [Abstract][Full Text] [Related]
18. Catalytic enantioselective amide allylation of isatins and its application in the synthesis of 2-oxindole derivatives spiro-fused to the α-methylene-γ-butyrolactone functionality.
Takahashi M; Murata Y; Yagishita F; Sakamoto M; Sengoku T; Yoda H
Chemistry; 2014 Aug; 20(35):11091-100. PubMed ID: 25049083
[TBL] [Abstract][Full Text] [Related]
19. Catalytic Enantioselective 1,3-Alkyl Shift in Alkyl Aryl Ethers: Efficient Synthesis of Optically Active 3,3'-Diaryloxindoles.
Gade AB; Bagle PN; Shinde PS; Bhardwaj V; Banerjee S; Chande A; Patil NT
Angew Chem Int Ed Engl; 2018 May; 57(20):5735-5739. PubMed ID: 29573526
[TBL] [Abstract][Full Text] [Related]
20. Stereochemical surprises in the Lewis acid-mediated allylation of isatins.
Vyas DJ; Fröhlich R; Oestreich M
J Org Chem; 2010 Oct; 75(19):6720-3. PubMed ID: 20825233
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
