Gotowe bibliografie tematyczne / 3-disubstituted oxindoles / Artykuły w czasopismach
Kliknij ten link, aby zobaczyć inne rodzaje publikacji na ten temat: 3-disubstituted oxindoles.

Artykuły w czasopismach na temat „3-disubstituted oxindoles”

Autor: Grafiati
Data publikacji: 6 września 2023

Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych

Wybierz rodzaj źródła:

Sprawdź 50 najlepszych artykułów w czasopismach naukowych na temat „3-disubstituted oxindoles”.

Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.

Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.

Przeglądaj artykuły w czasopismach z różnych dziedzin i twórz odpowiednie bibliografie.

1

Ortega-Martínez, Aitor, Cynthia Molina, Cristina Moreno-Cabrerizo, José Sansano i Carmen Nájera. "Synthesis of 3,3-Disubstituted 2-Oxindoles by Deacylative Alkylation of 3-Acetyl-2-oxindoles". Synthesis 49, nr 23 (22.08.2017): 5203–10. http://dx.doi.org/10.1055/s-0036-1590880.

Pełny tekst źródła
Streszczenie:
An innovative and efficient monoalkylation and nonsymmetrical 3,3-dialkylation of oxindoles has been achieved. First, the monoalkylation of 3-acetyl-2-oxindoles can be performed in good yields under mild reaction conditions using alkyl halides and benzyltrimethylammonium hydroxide (Triton B) as base at room temperature. This methodology is applied to construct the synthetically challenging compound 1,3-dimethyl-2-oxindole. Subsequent deacylative alkylation (DaA) of the alkylated 3-acetyl-2-oxindoles with alkyl halides takes place efficiently using LiOEt or by conjugate addition with electron-deficient alkenes in the presence of Triton B at room temperature under argon, affording the corresponding unsymmetrically 3,3-disubstituted 2-oxindoles. This simple methodology has been applied to the synthesis of precursors of horsfiline, esermethole, physostigmine, and phenserine alkaloids.
Style APA, Harvard, Vancouver, ISO itp.
2

Cui, Bao-Dong, Yong You, Jian-Qiang Zhao, Jian Zuo, Zhi-Jun Wu, Xiao-Ying Xu, Xiao-Mei Zhang i Wei-Cheng Yuan. "3-Pyrrolyl-oxindoles as efficient nucleophiles for organocatalytic asymmetric synthesis of structurally diverse 3,3′-disubstituted oxindole derivatives". Chemical Communications 51, nr 4 (2015): 757–60. http://dx.doi.org/10.1039/c4cc08364d.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Ding, Zhengtian, i Wangqing Kong. "Synthesis of Carbonyl-Containing Oxindoles via Ni-Catalyzed Reductive Aryl-Acylation and Aryl-Esterification of Alkenes". Molecules 27, nr 18 (11.09.2022): 5899. http://dx.doi.org/10.3390/molecules27185899.

Pełny tekst źródła
Streszczenie:
Carbonyl-containing oxindoles are ubiquitous core structures present in many biologically active natural products and pharmaceutical molecules. Nickel-catalyzed reductive aryl-acylation of alkenes using aryl anhydrides or alkanoyl chlorides as acyl sources is developed, providing 3,3-disubstituted oxindoles bearing ketone functionality at the 3-position. Moreover, nickel-catalyzed reductive aryl-esterification of alkenes using chloroformate as ester sources is further developed, affording 3,3-disubstituted oxindoles bearing ester functionality at the 3-position. This strategy has the advantages of good yields and high functional group compatibility.
Style APA, Harvard, Vancouver, ISO itp.
4

Chen, Lin, Yong You, Ming-Liang Zhang, Jian-qiang Zhao, Jian Zuo, Xiao-Mei Zhang, Wei-Cheng Yuan i Xiao-Ying Xu. "Organocatalytic asymmetric Michael addition of 3-substituted oxindoles to α,β-unsaturated acyl phosphonates for the synthesis of 3,3′-disubstituted oxindoles with chiral squaramides". Organic & Biomolecular Chemistry 13, nr 15 (2015): 4413–17. http://dx.doi.org/10.1039/c5ob00317b.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Cheng, Wen-Fu, Ling-Yan Chen, Fang-Fang Xu, Wei-Yu Lin, Xinfeng Ren i Ya Li. "Organocatalytic asymmetric Michael addition between 3-subsituted oxindoles and enals catalyzed by camphor sulfonyl hydrazine". Organic & Biomolecular Chemistry 17, nr 4 (2019): 885–91. http://dx.doi.org/10.1039/c8ob02934b.

Pełny tekst źródła
Streszczenie:
3,3-Disubstituted oxindoles containing vicinal stereogenic carbon centers have been synthesized through organocatalytic asymmetric Michael addition between 3-substituted oxindoles and enals catalyzed by chiral camphor sulfonyl hydrazines (CaSHs).
Style APA, Harvard, Vancouver, ISO itp.
6

Rao, Madhuri P., Shubha S. Gunaga, Johannes Zuegg, Rambabu Pamarthi i Madhu Ganesh. "Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes". Organic & Biomolecular Chemistry 17, nr 42 (2019): 9390–402. http://dx.doi.org/10.1039/c9ob01429b.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Zhang, Chun-Lin, You-Feng Han i Song Ye. "N-Heterocyclic carbene-catalyzed β-addition of enals to 3-alkylenyloxindoles: synthesis of oxindoles with all-carbon quaternary stereocenters". Chemical Communications 55, nr 55 (2019): 7966–69. http://dx.doi.org/10.1039/c9cc03099a.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Krishnan, Shyam, i Brian M. Stoltz. "Preparation of 3,3-disubstituted oxindoles by addition of malonates to 3-halo-3-oxindoles". Tetrahedron Letters 48, nr 43 (październik 2007): 7571–73. http://dx.doi.org/10.1016/j.tetlet.2007.08.131.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Li, Man, Fu-Sheng He, Long-Shan Ji, Ya-Ting Gao, Xin Zhang, Zhuo Yu, Miao Fang, Jie Wu i Yue-Qiu Gao. "Synthesis and biological evaluation of fluorinated 3,4-dihydroquinolin-2(1H)-ones and 2-oxindoles for anti-hepatic fibrosis". RSC Advances 11, nr 11 (2021): 5923–27. http://dx.doi.org/10.1039/d0ra09430g.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Cao, An-Zhu, Yu-Ting Xiao, Yan-Chen Wu, Ren-Jie Song, Ye-Xiang Xie i Jin-Heng Li. "Copper-catalyzed C–H [3 + 2] annulation of N-substituted anilines with α-carbonyl alkyl bromides via C(sp3)–Br/C(sp2)–H functionalization". Organic & Biomolecular Chemistry 18, nr 11 (2020): 2170–74. http://dx.doi.org/10.1039/d0ob00399a.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
11

Xu, Lubin, Haohua Chen, Jian Liu, Lan Zhou, Qing Liu, Yu Lan i Jian Xiao. "Chiral phosphoric acid-catalyzed asymmetric C(sp3)–H functionalization of biomass-derived 2,5-dimethylfuran via two sequential Cope-type rearrangements". Organic Chemistry Frontiers 6, nr 8 (2019): 1162–67. http://dx.doi.org/10.1039/c8qo01375f.

Pełny tekst źródła
Streszczenie:
The first organocatalytic asymmetric C(sp3)–H functionalization of biomass-derived 2,5-dimethylfuran with alcohols to afford enantioenriched furan-derived 3,3′-disubstituted oxindoles in high enantioselectivity.
Style APA, Harvard, Vancouver, ISO itp.
12

Liu, Yong-Liang, Xiao-Ping Wang, Jie Wei i Ya Li. "Synthesis of oxindoles bearing a stereogenic 3-fluorinated carbon center from 3-fluorooxindoles". Organic & Biomolecular Chemistry 20, nr 3 (2022): 538–52. http://dx.doi.org/10.1039/d1ob01964c.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
13

Wang, Juanjuan, Danfeng Huang, Ke-Hu Wang, Xiansha Peng, Yingpeng Su, Yulai Hu i Ying Fu. "Tin powder-promoted one-pot synthesis of 3-spiro-fused or 3,3′-disubstituted 2-oxindoles". Organic & Biomolecular Chemistry 14, nr 40 (2016): 9533–42. http://dx.doi.org/10.1039/c6ob01487a.

Pełny tekst źródła
Streszczenie:
A convenient and efficient method for the constructions of 3-spirooxindole derivatives or 3,3′-disubstituted oxindoles has been developed from one-pot reactions of isatins, hydrazides or aromatic amines, 2-(bromomethyl)acrylic ester in the presence of a catalytic amount of Brønsted or Lewis acid promoted by tin powder instead of toxic stannanes.
Style APA, Harvard, Vancouver, ISO itp.
14

Nakazaki, Atsuo, Keitaro Miyagawa i Toshio Nishikawa. "Diastereoselective Synthesis of 3,3-Disubstituted Oxindoles from N-Aryl-3-Chlorooxindoles Bearing C–N Axial Chirality via Nucleo­philic Substitution". Synlett 26, nr 08 (24.02.2015): 1116–20. http://dx.doi.org/10.1055/s-0034-1380266.

Pełny tekst źródła
Streszczenie:
Diastereoselective synthesis of 3,3-disubstituted oxindoles was examined using racemic N-aryl-3-chlorooxindoles bearing C–N axial chirality. The reaction involved the nucleophilic substitution of 3-chlorooxindoles via an ortho-azaxylylene intermediate in the presence of AgBF4 and MS 4 Å. High diastereoselectivities (up to >95:<5) were achieved in the formation of 3-alkyl-3-aryloxindole derivatives when electron-rich arenes were used.
Style APA, Harvard, Vancouver, ISO itp.
15

Devi, Manju, Amol P. Jadhav i Ravi P. Singh. "KOH-mediated stereoselective alkylation of 3-bromooxindoles for the synthesis of 3,3′-disubstituted oxindoles with two contiguous all carbon quaternary centres". New Journal of Chemistry 45, nr 19 (2021): 8445–48. http://dx.doi.org/10.1039/d0nj06283a.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
16

Deng, Fei, Shin A. Moteki i Keiji Maruoka. "Catalytic Asymmetric Alkylation of 3-Aryl-Substituted Oxindoles to give 3,3-Disubstituted Oxindoles under Phase-Transfer Conditions". Asian Journal of Organic Chemistry 3, nr 4 (12.03.2014): 395–98. http://dx.doi.org/10.1002/ajoc.201400011.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
17

Feng, Ting-Ting, Xuan Huang, Xiong-Li Liu, De-Hong Jing, Xiong-Wei Liu, Feng-Ming Guo, Ying Zhou i Wei-Cheng Yuan. "Highly regioselective synthesis of 3-alkenyl-oxindole ring-fused 3,3′-disubstituted oxindoles via direct gamma-substitution of Morita–Baylis–Hillman carbonates of isatins with 3-substituted oxindoles". Org. Biomol. Chem. 12, nr 46 (2.10.2014): 9366–74. http://dx.doi.org/10.1039/c4ob01523a.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
18

Meerakrishna, Ramakrishnan Suseela, Suresh Snoxma Smile, Mohanakumaran Athira, Venkata Surya Kumar Choutipalli i Ponnusamy Shanmugam. "Diverse reactivity of isatin-based N,N′-cyclic azomethine imine dipoles with arynes: synthesis of 1′-methyl-2′-oxospiro [indene-1,3′-indolines] and 3-aryl-3-pyrazol-2-oxindoles". New Journal of Chemistry 44, nr 27 (2020): 11593–601. http://dx.doi.org/10.1039/d0nj01684e.

Pełny tekst źródła
Streszczenie:
Reaction of aryne with isatin based N,N′-cyclic AMI 1,3-dipole afforded 3,3-disubstituted oxindole while methyl substitution on the pyrrolidine ring of 1,3-dipole directed [3+2] cycloaddition products.
Style APA, Harvard, Vancouver, ISO itp.
19

Deng, Fei, Shin A. Moteki i Keiji Maruoka. "ChemInform Abstract: Catalytic Asymmetric Alkylation of 3-Aryl-Substituted Oxindoles to Give 3,3-Disubstituted Oxindoles under Phase-Transfer Conditions." ChemInform 45, nr 45 (23.10.2014): no. http://dx.doi.org/10.1002/chin.201445125.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
20

Cui, Bao-Dong, Yong You, Jian-Qiang Zhao, Jian Zuo, Zhi-Jun Wu, Xiao-Ying Xu, Xiao-Mei Zhang i Wei-Cheng Yuan. "ChemInform Abstract: 3-Pyrrolyl-Oxindoles as Efficient Nucleophiles for Organocatalytic Asymmetric Synthesis of Structurally Diverse 3,3′-Disubstituted Oxindole Derivatives." ChemInform 46, nr 23 (22.05.2015): no. http://dx.doi.org/10.1002/chin.201523124.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
21

Zuo, Jian, Zhi-Jun Wu, Jian-Qiang Zhao, Ming-Qiang Zhou, Xiao-Ying Xu, Xiao-Mei Zhang i Wei-Cheng Yuan. "Preparation of 3-Sulfonylated 3,3-Disubstituted Oxindoles by the Addition of Sulfinate Salts to 3-Halooxindoles". Journal of Organic Chemistry 80, nr 1 (8.12.2014): 634–40. http://dx.doi.org/10.1021/jo502270a.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
22

Song, Xiang-Jia, Hong-Xia Ren, Min Xiang, Chen-Yi Li, Ying Zou, Xia Li, Zhi-Cheng Huang, Fang Tian i Li-Xin Wang. "Organocatalytic Enantioselective Michael Addition between 3-(3-hydroxy-1H-pyrazol-1-yl)Oxindole and β-Nitrostyrene for the Preparation of Chiral Disubstituted Oxindoles". Journal of Organic Chemistry 85, nr 14 (25.06.2020): 9290–300. http://dx.doi.org/10.1021/acs.joc.9b03337.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
23

Kaur, Jasneet, Anita Kumari i Swapandeep Singh Chimni. "Grinding assisted, column chromatography free decarboxylative carbon-carbon bond formation: Greener synthesis of 3, 3-disubstituted oxindoles". Tetrahedron 73, nr 6 (luty 2017): 802–8. http://dx.doi.org/10.1016/j.tet.2016.12.070.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
24

Lee, Hyun Ju, Ko Hoon Kim, Se Hee Kim i Jae Nyoung Kim. "Palladium-catalyzed oxidative arylation of trisubstituted olefin: an efficient synthesis of 3-(disubstituted)alkylidene-oxindoles". Tetrahedron Letters 54, nr 2 (styczeń 2013): 170–75. http://dx.doi.org/10.1016/j.tetlet.2012.10.122.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
25

Jia, Shi-Kun, Long-Long Song, Yu-Bing Lei, A. Gopi Krishna Reddy, Dong Xing i Wen-Hao Hu. "A Rh(ii)-catalyzed three-component reaction of 3-diazooxindoles with N,N-disubstituted anilines and glyoxylates for the synthesis of 3-aryl-3-substituted oxindoles". Organic & Biomolecular Chemistry 14, nr 43 (2016): 10157–60. http://dx.doi.org/10.1039/c6ob01907b.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
26

Zuo, Jian, Zhi-Jun Wu, Jian-Qiang Zhao, Ming-Qiang Zhou, Xiao-Ying Xu, Xiao-Mei Zhang i Wei-Cheng Yuan. "ChemInform Abstract: Preparation of 3-Sulfonylated 3,3-Disubstituted Oxindoles by the Addition of Sulfinate Salts to 3-Halooxindoles." ChemInform 46, nr 22 (15.05.2015): no. http://dx.doi.org/10.1002/chin.201522152.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
27

You, Yong, Zhi-Jun Wu, Zhen-Hua Wang, Xiao-Ying Xu, Xiao-Mei Zhang i Wei-Cheng Yuan. "Enantioselective Synthesis of 3,3-Disubstituted Oxindoles Bearing Two Different Heteroatoms at the C3 Position by Organocatalyzed Sulfenylation and Selenenylation of 3-Pyrrolyl-oxindoles". Journal of Organic Chemistry 80, nr 16 (12.08.2015): 8470–77. http://dx.doi.org/10.1021/acs.joc.5b01491.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
28

Wu, Chongyang, Guofeng Li, Wangsheng Sun, Ming Zhang, Liang Hong i Rui Wang. "Organocatalytic Highly Enantioselective Monofluoroalkylation of 3-Bromooxindoles: Construction of Fluorinated 3,3′-Disubstituted Oxindoles and Their Derivatives". Organic Letters 16, nr 7 (18.03.2014): 1960–63. http://dx.doi.org/10.1021/ol500517d.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
29

Kim, Ko Hoon, Hye Ran Moon, Junseong Lee i Jae Nyoung Kim. "Palladium-Catalyzed Construction of Spirooxindoles by Arylative Cyclization of 3-(γ,δ-Disubstituted)allylidene-2-Oxindoles". Advanced Synthesis & Catalysis 357, nr 4 (4.02.2015): 701–8. http://dx.doi.org/10.1002/adsc.201400965.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
30

Lee, Hyun Ju, Ko Hoon Kim, Se Hee Kim i Jae Nyoung Kim. "ChemInform Abstract: Palladium-Catalyzed Oxidative Arylation of Trisubstituted Olefin: An Efficient Synthesis of 3-(Disubstituted)alkylidene-oxindoles." ChemInform 44, nr 15 (25.03.2013): no. http://dx.doi.org/10.1002/chin.201315107.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
31

Kókai, Eszter, Gyula Simig i Balázs Volk. "Literature Survey and Further Studies on the 3-Alkylation of N-Unprotected 3-Monosubstituted Oxindoles. Practical Synthesis of N-Unprotected 3,3-Disubstituted Oxindoles and Subsequent Transformations on the Aromatic Ring". Molecules 22, nr 1 (26.12.2016): 24. http://dx.doi.org/10.3390/molecules22010024.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
32

Chen, Lin, Yong You, Ming-Liang Zhang, Jian-qiang Zhao, Jian Zuo, Xiao-Mei Zhang, Wei-Cheng Yuan i Xiao-Ying Xu. "ChemInform Abstract: Organocatalytic Asymmetric Michael Addition of 3-Substituted Oxindoles to α,β-Unsaturated Acyl Phosphonates for the Synthesis of 3,3′-Disubstituted Oxindoles with Chiral Squaramides." ChemInform 46, nr 34 (sierpień 2015): no. http://dx.doi.org/10.1002/chin.201534147.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
33

Pathan, Mohsinkhan Y., Santosh S. Chavan, Taufeekaslam M. Y. Shaikh, Shridhar H. Thorat, Rajesh G. Gonnade i Shafeek A. R. Mulla. "Facile One-Pot Multi-Component Synthesis of Spirooxindoles and 3, 3’-Disubstituted Oxindoles via sp3 C-H Activation/Functionalization of Azaarenes". ChemistrySelect 2, nr 28 (29.09.2017): 9147–52. http://dx.doi.org/10.1002/slct.201701507.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
34

Zuo, Jian, Yu-Hua Liao, Xiao-Mei Zhang i Wei-Cheng Yuan. "Organocatalyzed Enantioselective Decarboxylative Stereoablation Reaction for the Construction of 3,3′-Disubstituted Oxindoles Using β-Ketoacids and 3-Halooxindoles". Journal of Organic Chemistry 77, nr 24 (7.12.2012): 11325–32. http://dx.doi.org/10.1021/jo302048v.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
35

Kim, Ko Hoon, Hye Ran Moon, Junseong Lee i Jae Nyoung Kim. "ChemInform Abstract: Palladium-Catalyzed Construction of Spirooxindoles by Arylative Cyclization of 3-(γ,δ-Disubstituted)allylidene-2-Oxindoles." ChemInform 46, nr 31 (16.07.2015): no. http://dx.doi.org/10.1002/chin.201531140.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
36

Wu, Chongyang, Guofeng Li, Wangsheng Sun, Ming Zhang, Liang Hong i Rui Wang. "ChemInform Abstract: Organocatalytic Highly Enantioselective Monofluoroalkylation of 3-Bromooxindoles: Construction of Fluorinated 3,3′-Disubstituted Oxindoles and Their Derivatives." ChemInform 45, nr 37 (28.08.2014): no. http://dx.doi.org/10.1002/chin.201437132.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
37

Liu, Xiong-Wei, Zhen Yao, Guan-Lian Wang, Zhi-Yong Chen, Xiong-Li Liu, Min-Yi Tian, Qi-Di Wei, Ying Zhou i Jian-Fei Zhang. "Efficient 1,6-addition reactions of 3-substituted oxindoles: Access to isoxazole-fused 3,3′-disubstituted oxindole scaffolds and hexahydro-1h-pyrido[2,3-b]indol-2-one scaffolds". Synthetic Communications 48, nr 12 (23.05.2018): 1454–64. http://dx.doi.org/10.1080/00397911.2018.1454475.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
38

Zhou, Rong, Rongfang Liu, Kai Zhang, Ling Han, Honghui Zhang, Wenchao Gao i Ruifeng Li. "Metal-free formal carbon–halogen bond insertion: facile syntheses of 3-halo 3,3′-disubstituted oxindoles and spirooxindole-γ-butyrolactones". Chemical Communications 53, nr 51 (2017): 6860–63. http://dx.doi.org/10.1039/c7cc03765a.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
39

Moon, Hye Ran, Ko Hoon Kim, Junseong Lee i Jae Nyoung Kim. "Synthesis of 3-(γ,δ-Disubstituted)allylidene-2-Oxindoles from Isatins by Wittig Reaction with Morita-Baylis-Hillman Bromides". Bulletin of the Korean Chemical Society 36, nr 1 (styczeń 2015): 219–25. http://dx.doi.org/10.1002/bkcs.10053.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
40

Ohmatsu, Kohsuke, Yuichiro Ando i Takashi Ooi. "Asymmetric Substitution at the Tetrasubstituted Chiral Carbon: Catalytic Ring-Opening Alkylation of Racemic 2,2-Disubstituted Aziridines with 3-Substituted Oxindoles". Journal of the American Chemical Society 135, nr 50 (10.12.2013): 18706–9. http://dx.doi.org/10.1021/ja411647x.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
41

Wang, Dong-Chao, Hai-Xia Wang, Er-Jun Hao, Xiao-Han Jiang, Ming-Sheng Xie, Gui-Rong Qu i Hai-Ming Guo. "Synthesis of 3,3-Disubstituted Oxindoles Containing a 3-(4-Aminobut-2-ynyl) Unit via Domino Heck-Sonogashira Reaction in Water". Advanced Synthesis & Catalysis 358, nr 3 (18.01.2016): 494–99. http://dx.doi.org/10.1002/adsc.201500887.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
42

Zuo, Jian, Yu-Hua Liao, Xiao-Mei Zhang i Wei-Cheng Yuan. "ChemInform Abstract: Organocatalyzed Enantioselective Decarboxylative Stereoablation Reaction for the Construction of 3,3′-Disubstituted Oxindoles Using β-Ketoacids and 3-Halooxindoles." ChemInform 44, nr 22 (13.05.2013): no. http://dx.doi.org/10.1002/chin.201322114.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
43

You, Yong, Zhi-Jun Wu, Jian-Feng Chen, Zhen-Hua Wang, Xiao-Ying Xu, Xiao-Mei Zhang i Wei-Cheng Yuan. "Organocatalytic Asymmetric Michael Addition of 3-Pyrrolyloxindoles to β-Phthalimidonitroethene for the Synthesis of 3,3′-Disubstituted Oxindoles Bearing Contiguous 3,α,β-Triamino Functionality". Journal of Organic Chemistry 81, nr 13 (17.06.2016): 5759–65. http://dx.doi.org/10.1021/acs.joc.6b00896.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
44

MORENO-CABRERIZO, CRISTINA, AITOR ORTEGA-MARTÍNEZ, CYNTHIA MOLINA, CARMEN NÁJERA i JOSÉ M. SANSANO. "Deacylative alkylation (DaA) of N-methyl-3-acetyl-2-oxindole for the synthesis of symmetrically 3,3-disubstituted 2-oxindoles. An access gate to anticancer agents and natural products." Anais da Academia Brasileira de Ciências 90, nr 1 suppl 2 (2018): 1089–99. http://dx.doi.org/10.1590/0001-3765201820170783.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
45

Ohmatsu, Kohsuke, Yuichiro Ando i Takashi Ooi. "ChemInform Abstract: Asymmetric Substitution at the Tetrasubstituted Chiral Carbon: Catalytic Ring-Opening Alkylation of Racemic 2,2-Disubstituted Aziridines with 3-Substituted Oxindoles." ChemInform 45, nr 27 (20.06.2014): no. http://dx.doi.org/10.1002/chin.201427114.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
46

Wang, Dong-Chao, Hai-Xia Wang, Er-Jun Hao, Xiao-Han Jiang, Ming-Sheng Xie, Gui-Rong Qu i Hai-Ming Guo. "Cover Picture: Synthesis of 3,3-Disubstituted Oxindoles Containing a 3-(4-Aminobut-2-ynyl) Unit via Domino Heck-Sonogashira Reaction in Water (Adv. Synth. Catal. 3/2016)". Advanced Synthesis & Catalysis 358, nr 3 (2.02.2016): 506. http://dx.doi.org/10.1002/adsc.201600052.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
47

Wang, Xiaogang, Jin Zhang, Yuan He, Di Chen, Chao Wang, Fangzhou Yang, Weitao Wang, Yangmin Ma i Michal Szostak. "Ruthenium(II)-Catalyzed Ortho-C–H Alkylation of Naphthylamines with Diazo Compounds for Synthesis of 2,2-Disubstituted π-Extended 3-Oxindoles in Water". Organic Letters 22, nr 13 (19.06.2020): 5187–92. http://dx.doi.org/10.1021/acs.orglett.0c01811.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
48

Piemontesi, Cyril, Qian Wang i Jieping Zhu. "Synthesis of 3,3-disubstituted oxindoles by one-pot integrated Brønsted base-catalyzed trichloroacetimidation of 3-hydroxyoxindoles and Brønsted acid-catalyzed nucleophilic substitution reaction". Organic & Biomolecular Chemistry 11, nr 9 (2013): 1533. http://dx.doi.org/10.1039/c2ob27196f.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
49

Piemontesi, Cyril, Qian Wang i Jieping Zhu. "ChemInform Abstract: Synthesis of 3,3-Disubstituted Oxindoles by One-Pot Integrated Broensted Base-Catalyzed Trichloroacetimidation of 3-Hydroxyoxindoles and Broensted Acid-Catalyzed Nucleophilic Substitution Reaction." ChemInform 44, nr 29 (1.07.2013): no. http://dx.doi.org/10.1002/chin.201329113.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
50

Kim, Su Yeon, Sangku Lee, Gieun Kim, Beom Kyu Min i Jae Nyoung Kim. "Synthesis of 3-(β,δ-Disubstituted)allylidene-2-oxindoles by SN 2′ Reaction of Phosphorous Ylides with Carbonates of Isatin-derived Moritas-Baylis-Hillman Adducts". Bulletin of the Korean Chemical Society 38, nr 9 (21.07.2017): 1097–100. http://dx.doi.org/10.1002/bkcs.11193.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Oferujemy zniżki na wszystkie plany premium dla autorów, których prace zostały uwzględnione w tematycznych zestawieniach literatury. Skontaktuj się z nami, aby uzyskać unikalny kod promocyjny!

Do bibliografii