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1. Full Text Regioselective Friedel–Crafts Reaction of Electron‐Rich Benzenoid Arenes and Spiroepoxyoxindole at the Spiro‐Centre: Efficient Synthesis of Benzofuroindolines and 2H‐ Spiro[benzofuran]‐3,3′‐oxindoles
by Hajra, Saumen and Maity, Subrata and Roy, Sayan
Advanced Synthesis & Catalysis, ISSN 1615-4150, 07/2016, Volume 358, Issue 14, pp. 2300 - 2306
Metal triflate‐catalysed intermolecular Friedel–Crafts reactions involving electron‐rich benzenoid arenes and spiroepoxyoxindoles at the spiro‐centre have been... 
Friedel–Crafts reaction | benzofuroindolines | spiroepoxyoxindoles | benzenoid arenes | spiro[benzofuran]‐3,3′‐oxindoles | 3‐aryl‐3‐(hydroxymethyl)oxindoles | 3-aryl-3-(hydroxymethyl)oxindoles | spiro[benzofuran]-3,3′-oxindoles | N-ACETYL INDOLES | ASYMMETRIC-SYNTHESIS | DIAZONAMIDE-A | LEWIS-ACID | CHEMISTRY, ORGANIC | 2ND TOTAL-SYNTHESIS | spiro[benzofuran]-3,3 '-oxindoles | EPOXIDES | ARYL | STEREOSELECTIVE-SYNTHESIS | CHEMISTRY, APPLIED | Friedel-Crafts reaction | CYCLIZATION | ALKYLATION REACTION | Synthesis (chemistry) | Synthesis | Aromatic compounds | Benzenoids | Phenols | Catalysis | Ring opening
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2. Full Text Synthesis of Deoxyaminosugar Cyclohexyl-L-callipeltose and Its Diastereomer Using Pd-Catalyzed Asymmetric Hydroalkoxylation
by Lee, S and Rhee, YH
JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, 07/2019, Volume 84, Issue 14, pp. 9353 - 9357
Cyclohexyl-L-callipeltose, an aminodeoxysugar subunit of Callipeltoside A, was synthesized in six steps and 40% overall yield from readily available... 
OXINDOLES | CHEMISTRY, ORGANIC | SUGAR
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3. Full Text Catalytic Asymmetric [3+2] Cyclization Reactions of 3-lsothiocyanato Oxindoles and Alkynyl Ketones Via an in Situ Generated Magnesium Catalyst
by Wang, LQ and Yang, DX and Li, D and Liu, XH and Zhao, Q and Zhu, RR and Zhang, BZ and Wang, R
ORGANIC LETTERS, ISSN 1523-7060, 09/2015, Volume 17, Issue 17, pp. 4260 - 4263
A highly enantioselective formal [3 + 2] cycloaddition reaction between 3-isothiocyanato oxindoles and alkynyl ketones is reported for the first time. An... 
ISOTHIOCYANATO OXINDOLES | MANNICH-TYPE REACTION | ENANTIOSELECTIVE SYNTHESIS | 3-ISOTHIOCYANATO OXINDOLES | CHEMISTRY, ORGANIC | SPIROCYCLIC OXINDOLES | MICHAEL/CYCLIZATION REACTION | MICHAEL ADDITION/CYCLIZATION | POLYCYCLIC SPIROOXINDOLES | AMINO-THIOCARBAMATE CATALYSTS | HIGHLY EFFICIENT
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4. Full Text Catalytic functionalization of tertiary alcohols to fully substituted carbon centres
by Chen, Long and Yin, Xiao-Ping and Wang, Cui-Hong and Zhou, Jian
Organic and Biomolecular Chemistry, ISSN 1477-0520, 08/2014, Volume 12, Issue 32, pp. 6033 - 6048
The catalytic nucleophilic substitution of tertiary alcohols using carbon. or heteroatom based nucleophiles is a versatile methodology for the efficient,... 
3,3-DISUBSTITUTED OXINDOLES | NUCLEOPHILIC-SUBSTITUTION | ALPHA-HYDROXYKETONES | CHEMISTRY, ORGANIC | SPIROCYCLIC OXINDOLES | ORGANOCATALYTIC ASYMMETRIC-SYNTHESIS | FRIEDEL-CRAFTS ALKYLATION | ENANTIOSELECTIVE CONSTRUCTION | FACILE PREPARATION | RITTER REACTION | 3-SUBSTITUTED OXINDOLES | Alcohols - chemistry | Catalysis | Stereoisomerism | Carbon - chemistry
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5. Full Text The Squaramide‐Catalyzed 1,3‐Dipolar Cycloaddition of Nitroalkenes with N‐2,2,2‐Trifluoroethylisatin Ketimines: An Approach for the Synthesis of 5′‐Trifluoromethyl‐spiro[pyrrolidin‐3,2′‐oxindoles]
by Sun, Quantao and Li, Xiaoyuan and Su, Jinhuan and Zhao, Long and Ma, Mingxia and Zhu, Yuanyuan and Zhao, Yanyan and Zhu, Ranran and Yan, Wenjin and Wang, Kairong and Wang, Rui
Advanced Synthesis & Catalysis, ISSN 1615-4150, 10/2015, Volume 357, Issue 14‐15, pp. 3187 - 3196
A Cinchona alkaloid‐derived squaramide‐catalyzed asymmetric cycloaddition of trfluoromethyl‐containing azomethine ylides with β‐nitroalkenes was realized under... 
1,3‐dipolar cycloaddition | squaramides | 5′‐trifluoromethyl‐spiro‐[pyrrolidin‐3,2′‐oxindoles] | trifluoromethyl‐containing azomethine ylides | 5′-trifluoromethyl-spiro-[pyrrolidin-3,2′-oxindoles] | 1,3-dipolar cycloaddition | trifluoromethyl-containing azomethine ylides | CHIRAL SQUARAMIDES | ASYMMETRIC ONE-POT | AZOMETHINE YLIDES | CHEMISTRY, ORGANIC | 5 '-trifluoromethyl-spiro-[pyrrolidin-3,2 '-oxindoles] | SELECTIVE 3+2 CYCLOADDITION | CONTIGUOUS STEREOCENTERS | ENANTIOSELECTIVE MICHAEL ADDITION | MEDICINAL CHEMISTRY | ISOTHIOCYANATO OXINDOLES | DIVERSITY-ORIENTED SYNTHESIS | CHEMISTRY, APPLIED | CONJUGATE ADDITION | Cycloaddition | Synthesis | Catalysis | Asymmetry | Imines
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6. Full Text Recent advances in the synthesis of biologically active spirooxindoles
by Santos, Maria M.M
Tetrahedron, ISSN 0040-4020, 12/2014, Volume 70, Issue 52, pp. 9735 - 9757
Display Omitted 
Spirooxindoles | Cycloaddition | Spiro alkaloids | Biological activity | SPIRO QUATERNARY CENTERS | ENANTIOSELECTIVE SYNTHESIS | 3-ISOTHIOCYANATO OXINDOLES | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | SPIROCYCLIC OXINDOLES | HIGHLY EFFICIENT | ASYMMETRIC 3+2 ANNULATION | DIVERSITY-ORIENTED SYNTHESIS | 1,3-DIPOLAR CYCLOADDITION | STEREOSELECTIVE-SYNTHESIS | Tetrahedrons | Synthesis (chemistry)
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7. Full Text Oxindole synthesis by direct coupling of Csp2-H and C sp3-H centers
by Jia, Yi-Xia and Kündig, E. Peter
Angewandte Chemie - International Edition, ISSN 1433-7851, 02/2009, Volume 48, Issue 9, pp. 1636 - 1639
Oxindoles | Radical reactions | Copper | Oxidative coupling
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8. Full Text Diastereoselective construction of pyrrolo[2,1-a]isoquinoline-based bispirooxindoles through a three-component [3 + 2] cycloaddition
by Guo, Jiaomei and Zhao, Yang and Fang, Dongmei and Wang, Qilin and Bu, Zhanwei
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2018, Volume 16, Issue 33, pp. 6025 - 6034
An efficient three-component one-pot [3 + 2] cycloaddition of isatins, 1,2,3,4-tetrahydroisoquinolines and methyleneindolinones has been developed. This... 
ISOTHIOCYANATO OXINDOLES | DIELS-ALDER REACTION | 3-ISOTHIOCYANATO OXINDOLES | 1,3-DIPOLAR CYCLOADDITION | SPIROCYCLOPENTANE OXINDOLES | BIOLOGY-ORIENTED SYNTHESIS | AZOMETHINE YLIDES | CHEMISTRY, ORGANIC | KETAL SPIROOXINDOLES | ENANTIOSELECTIVE CONSTRUCTION | HIGHLY EFFICIENT | Stereoselectivity | Organic chemistry | Cycloaddition
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9. Full Text Catalytic Enantioselective Construction of Quaternary Stereocenters: Assembly of Key Building Blocks for the Synthesis of Biologically Active Molecules
by Liu, Yiyang and Han, Seo-Jung and Liu, Wen-Bo and Stoltz, Brian M
Accounts of Chemical Research, ISSN 0001-4842, 03/2015, Volume 48, Issue 3, pp. 740 - 751
CONSPECTUS: The ever-present demand for drugs with better efficacy and fewer side effects continually motivates scientists to explore the vast chemical space.... 
3,3-DISUBSTITUTED OXINDOLES | ASYMMETRIC CONJUGATE ADDITION | COMMUNESIN F | LIGANDS | NATURAL-PRODUCTS | ALLYLIC ALKYLATION | ENONES | ALPHA-ALLYLATION | TERTIARY | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | Oxindoles | Ketones - chemical synthesis | Stereoisomerism | Drug Design | Ketones - chemistry | Indoles - chemical synthesis | Lactams - chemical synthesis | Organometallic Compounds - chemistry | Molecular Structure | Catalysis | Indoles - chemistry | Lactams - chemistry | Research | Chemical properties | Nucleophilic reactions | Chemical synthesis | Alkylation | Enolates | Drugs | Construction | Ketones | Asymmetry | Catalysts | Nucleophiles
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10. Full Text Recent Advances in Asymmetric Organocatalytic Construction of 3,3′-Spirocyclic Oxindoles
by Hong, Liang and Wang, Rui
Advanced Synthesis and Catalysis, ISSN 1615-4150, 04/2013, Volume 355, Issue 6, pp. 1023 - 1052
The asymmetric organocatalysis is definitely one of the most powerful and versatile tools for the rapid construction of various spirocyclic oxindoles. In the... 
organocatalysis | asymmetric catalysis | spiro-oxindoles | stereoselectivity | HIGHLY ENANTIOSELECTIVE SYNTHESIS | DIELS-ALDER REACTIONS | CHEMISTRY, ORGANIC | PICTET-SPENGLER REACTIONS | SPIROCYCLIC OXINDOLES | QUATERNARY CARBON STEREOCENTERS | INTRAMOLECULAR HECK REACTIONS | CATALYZED 3+2 ANNULATION | BAYLIS-HILLMAN CARBONATES | STEREOSELECTIVE-SYNTHESIS | CHEMISTRY, APPLIED | STRUCTURE-BASED DESIGN | Strategy | Construction | Synthesis | Catalysis | Asymmetry | Construction equipment
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11. Full Text Highly efficient construction of chiral dispirocyclic oxindole/thiobutyrolactam/chromanone complexes through Michael/cyclization cascade reactions with a rosin-based squaramide catalyst
by Lin, Ning and Long, Xian-wen and Chen, Qing and Chen, Kai-bin and Zhu, Wen-run and Wang, Bi-chuan and Jiang, Cai-wu and Weng, Jiang and Lu, Gui
Tetrahedron, ISSN 0040-4020, 07/2018, Volume 74, Issue 27, pp. 3734 - 3741
An efficient asymmetric Michael/cyclization cascade reaction of 4-chromanones with isothiocyanato oxindoles has been revealed. Under bifunctional... 
Chromanones | Rosin-based squaramide catalyst | Dispirocyclic oxindoles | 3-Isothiocyanato oxindoles | Asymmetric organocatalysis | MICHAEL REACTION | ENANTIOSELECTIVE SYNTHESIS | 3-ISOTHIOCYANATO OXINDOLES | CHEMISTRY, ORGANIC | BIFUNCTIONAL ORGANOCATALYSTS | SPIROOXINDOLES | 3-lsothiocyanato oxindoles | STEREOCENTERS | SEQUENCE | DERIVATIVES | CYCLIZATION | CONJUGATE ADDITION | Drugstores | Pharmacy | Catalysis
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12. Full Text Palladium-catalyzed one-pot approach to 3-(1,3-diarylprop- 2-YN-1-ylidene)oxindoles
by Lee, Jiyun and Park, Sunhwa and Shin, Kye Jung and Seo, Jae Hong
Politics and Religion Journal, ISSN 1820-6581, 2018, Volume 5, Issue 1, pp. 1795 - 1807
An efficient and stereoselective one-pot approach for synthesizing 3-(1,3-diarylprop-2-yn-1-ylidene)oxindoles has been developed, starting from propiolamide,... 
Oxindole | Heck Reaction | 3-(DIARYLMETHYLENE)OXINDOLES | CYCLIZATION REACTION | 3-ALKYLIDENEOXINDOLES | Sonogashira Reaction | 3-(Diarylprop-2-yn-1-ylidne)oxindole | OXINDOLES | CHEMISTRY, ORGANIC | ISOCYANATES | STEREOSELECTIVE-SYNTHESIS | Palladium Catalyst
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13. Full Text Highly enantioselective Michael addition of 3-arylthio- and 3-alkylthiooxindoles to nitroolefins catalyzed by a simple cinchona alkaloid derived phosphoramide
by Gao, Wei-Ming and Yu, Jin-Sheng and Zhao, Yu-Lei and Liu, Yun-Lin and Zhou, Feng and Wu, Hai-Hong and Zhou, Jian
Chemical Communications, ISSN 1359-7345, 12/2014, Volume 50, Issue 96, pp. 15179 - 15182
A new cinchona alkaloid derived bifunctional tertiary amine-phosphoramide C1e is identified as a highly enantioselective catalyst for Michael addition of both... 
BRONSTED ACID | MORITA-BAYLIS-HILLMAN | SYNERGISTIC ORGANOCATALYSIS | CONSTRUCTION | BOC-PROTECTED OXINDOLES | EFFICIENT SYNTHESIS | 3,3'-DISUBSTITUTED OXINDOLES | ORGANOCATALYTIC ASYMMETRIC-SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | 3-SUBSTITUTED OXINDOLES | SECONDARY AMINE | Catalysts | Alkaloids
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14. Full Text Highly enantioselective Michael addition of 3-arylthio- and 3-alkylthiooxindoles to nitroolefins catalyzed by a simple cinchona alkaloid derived phosphoramide
by Gao, Wei-Ming and Yu, Jin-Sheng and Zhao, Yu-Lei and Liu, Yun-Lin and Zhou, Feng and Wu, Hai-Hong and Zhou, Jian
Chemical communications (Cambridge, England), ISSN 1359-7345, 12/2014, Volume 50, Issue 96, pp. 15179 - 15182
A new cinchona alkaloid derived bifunctional tertiary amine-phosphoramide is identified as a highly enantioselective catalyst for Michael addition of both... 
Alkenes - chemistry | Phosphoramides - chemistry | Stereoisomerism | Sulfhydryl Compounds - chemistry | Catalysis | Indoles - chemistry | Cinchona Alkaloids - chemistry
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15. Full Text Synthesis of 3,3-Disubstituted Oxindoles by Palladium-Catalyzed Asymmetric Intramolecular -Arylation of Amides: Reaction Development and Mechanistic Studies
by Katayev, D and Jia, YX and Sharma, AK and Banerjee, D and Besnard, C and Sunoj, RB and Kundig, EP
CHEMISTRY-A EUROPEAN JOURNAL, ISSN 0947-6539, 09/2013, Volume 19, Issue 36, pp. 11916 - 11927
Palladium complexes incorporating chiral N-heterocyclic carbene (NHC) ligands catalyze the asymmetric intramolecular -arylation of amides producing... 
ENANTIOSELECTIVE SYNTHESIS | HETEROCYCLIC CARBENE LIGANDS | ALPHA-ARYLATION | HECK REACTIONS | asymmetric catalysis | QUATERNARY CARBON CENTERS | CHEMISTRY, MULTIDISCIPLINARY | 3-SUBSTITUTED OXINDOLES | arylation | ALDOL-TYPE REACTION | oxindoles | 3-ALLYL-3-ARYL OXINDOLES | COMPLEXES SYNTHESIS | palladium | IMIDAZOLIUM SALTS | N-heterocyclic carbenes | Amides | Palladium | Synthesis | Green technology | Organic compounds | Ligands | Asymmetry | Olefins | Transformations | Carbenes | Bonding
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16. Full Text Iron‐Catalyzed exo‐Selective Synthesis of Cyanoalkyl Indolines via Cyanoisopropylarylation of Unactivated Alkenes
by Li, Yanni and Chang, Yu and Li, Yufen and Cao, Cheng and Yang, Jinshuang and Wang, Baoling and Liang, Deqiang
Advanced Synthesis & Catalysis, ISSN 1615-4150, 07/2018, Volume 360, Issue 13, pp. 2488 - 2492
An iron‐catalyzed cyanoalkylation using azobisisobutyronitrile (AIBN) is reported. With unactivated double bond as the radical acceptor, N ‐allyl anilines... 
Azo compounds | Iron | Alkenes | Cyclization | Radical reactions | CONTAINING OXINDOLES | OXIDATIVE ARYLALKYLATION | N-ARYL ACRYLAMIDES | ALPHA,BETA-UNSATURATED KETONES | 3-ISOTHIOCYANATO OXINDOLES | CHEMISTRY, ORGANIC | ACTIVATED ALKENES | CYCLIZATION REACTION | ELECTRON-TRANSFER | SUBSTITUTED OXINDOLES | RADICAL CYCLIZATION | CHEMISTRY, APPLIED | Olefins | Chemical properties | Azobisisobutyronitrile | Heterocyclic compounds | Selectivity | Chemical synthesis | Substrates
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