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21. Full Text Palladium‐Catalyzed Asymmetric Construction of Vicinal Tertiary and All‐Carbon Quaternary Stereocenters by Allylation of β‐Ketocarbonyls with Morita–Baylis–Hillman Adducts
by Liu, Jiawang and Han, Zhaobin and Wang, Xiaoming and Meng, Fanye and Wang, Zheng and Ding, Kuiling
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2017, Volume 56, Issue 18, pp. 5050 - 5054
palladium | P ligands | asymmetric catalysis | spiro compounds | allylic compounds | P ligands
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22. Full Text Practical, efficient, and broadly applicable synthesis of readily differentiable vicinal diboronate compounds by catalytic three-component reactions
by Radomkit, Suttipol and Liu, Zhenxing and Closs, Anna and Mikus, Malte S and Hoveyda, Amir H
Tetrahedron, ISSN 0040-4020, 08/2017, Volume 73, Issue 33, pp. 5011 - 5017
Boron | Catalysis | Copper | Vicinal diboron compounds | Enantioselective synthesis | Allylic substitution | Chemical tests and reagents | Enantiomers | Olefins
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23. Full Text Synthesis of isothiosemicarbazones of potential antitumoral activity through a multicomponent reaction involving allylic bromides, carbonyl compounds and thiosemicarbazide
by Munaretto, Laiéli S and Ferreira, Misael and Gouvêa, Daniela P and Bortoluzzi, Adailton J and Assunção, Laura S and Inaba, Juliana and Creczynski-Pasa, Tânia B and Sá, Marcus M
Tetrahedron, ISSN 0040-4020, 06/2020, Volume 76, Issue 23, p. 131231
Isothiosemicarbazone | Green chemistry | Multicomponent reaction | Allylic bromide | Antitumoral activity
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24. Full Text Rationally Improved Chiral Brønsted Acid for Catalytic Enantioselective Allylboration of Aldehydes with an Expanded Reagent Scope
by Rauniyar, Vivek and Hall, Dennis G
Journal of organic chemistry, ISSN 0022-3263, 06/2009, Volume 74, Issue 11, pp. 4236 - 4241
Exact sciences and technology | Alicyclic compounds, terpenoids, prostaglandins, steroids | Alicyclic compounds | Preparations and properties | Aliphatic compounds | Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives | Organic chemistry | Chemistry | Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry | Heterocyclic compounds | General and physical chemistry | Catalysis | Catalysts: preparations and properties | Biological Products - chemical synthesis | Lactones - chemical synthesis | Stereoisomerism | Indicators and Reagents | Borates - chemistry | Methods | Aldehydes - chemistry | Carbonyl compounds | Allylic compounds | Chemical properties | Structure | Index Medicus
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25. Full Text Extremely Active Organocatalysts Enable a Highly Enantioselective Addition of Allyltrimethylsilane to Aldehydes
by Kaib, Philip S. J and Schreyer, Lucas and Lee, Sunggi and Properzi, Roberta and List, Benjamin
Angewandte Chemie (International ed.), ISSN 1433-7851, 10/2016, Volume 55, Issue 42, pp. 13200 - 13203
enantioselectivity | organocatalysis | silanes | nucleophilic addition | allylic compounds | Catalysis | Enantiomers | Aldehydes | Silane | Transformation | Catalysts | Test procedures | Moisture | Chemical reactions | Forming | Carbon | Substrates | Aliphatic compounds | Alcohols | Design | Asymmetry | Allyl compounds | Chemical synthesis
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26. Full Text Rhodium‐Catalyzed Enantioselective Intermolecular Hydroalkoxylation of Allenes and Alkynes with Alcohols: Synthesis of Branched Allylic Ethers
by Liu, Zi and Breit, Bernhard
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2016, Volume 55, Issue 29, pp. 8440 - 8443
allenes | synthetic methods | alkynes | allylic compounds | rhodium | Phosphates | Rhodium | Enantiomers | Alcohol | Aromatic compounds | Catalysis | Ethers | Chemical synthesis | Aliphatic compounds | Alkynes | Alcohols
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27. Full Text A highly regio- and stereo-selective [3+2] annulation of allylic compounds and 2-substituted 1,1-dicyanoalkenes through a catalytic carbon–phosphorus ylide reaction
by Feng, Jianqing and Lu, Xiyan and Kong, Aidi and Han, Xiuling
Tetrahedron, ISSN 0040-4020, 2007, Volume 63, Issue 26, pp. 6035 - 6041
Allylic compounds | Phosphine | 2-Substituted 1,1-dicyanoalkenes | Carbon–phosphorus ylide | Carbon-phosphorus ylide
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28. Full Text Stereoselective Construction of Quaternary Carbon Stereocenters via a Semipinacol Rearrangement Strategy
by Wang, Baomin and Tu, Yong Qiang
Accounts of chemical research, ISSN 0001-4842, 11/2011, Volume 44, Issue 11, pp. 1207 - 1222
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Alcohols - chemistry | Stereoisomerism | Cyclohexenes - chemistry | Epoxy Compounds - chemistry | Alkaloids - chemical synthesis | Molecular Structure | Catalysis | Carbon - chemistry | Chemistry Techniques, Synthetic - methods | Allylic compounds | Analysis | Rearrangements (Chemistry) | Epoxy compounds | Chemical bonds | Chemical properties | Research | Structure | Organic compounds | Construction | Migration | Chemists | Biocompatibility | Strategy | Carbon | Hydroxyl groups | Index Medicus
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29. Full Text Base‐Catalyzed One‐Pot Synthesis of Unsymmetrical Fluorenes from Aromatic ortho‐Dialdehydes and 1,3‐Dicarbonyl Compounds
by Seo, Ue Ryung and Chung, Young Keun and Lee, Chulbom
ChemCatChem, ISSN 1867-3880, 03/2016, Volume 8, Issue 6, pp. 1051 - 1054
fused-ring systems | domino reactions | fluorenes | hydrocarbons | allylic compounds | Physical Sciences | Chemistry | Chemistry, Physical | Science & Technology | Polycyclic aromatic hydrocarbons
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30. Full Text Recent advances in homogeneous metal-catalyzed aerobic C–H oxidation of benzylic compounds
by Urgoitia, Garazi and Martin, Raul San and Herrero, María Teresa and Domínguez, Esther
Catalysts, ISSN 2073-4344, 12/2018, Volume 8, Issue 12, p. 640
Molecular oxygen | Oxidation | Aryl ketones | Benzamides | Metal catalysts | Benzoate esters | Physical Sciences | Chemistry | Chemistry, Physical | Science & Technology | metal catalysts | oxidation | benzoate esters | benzamides | aryl ketones | molecular oxygen
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31. Full Text Et3B-mediated and palladium-catalyzed direct allylation of β-dicarbonyl compounds with Morita-Baylis-Hillman alcohols
by Abidi, Ahlem and Oueslati, Yosra and Rezgui, Farhat
Beilstein journal of organic chemistry, ISSN 1860-5397, 11/2016, Volume 12, Issue 1, pp. 2402 - 2409
Triethylborane | Palladium | Morita-Baylis-Hillman | Allylic substitution | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology | palladium | allylic substitution | triethylborane | Morita–Baylis–Hillman
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32. Full Text Allylic hydroxylation of triterpenoids by a plant cytochrome P450 triggers key chemical transformations that produce a variety of bitter compounds
by Takase, Shohei and Kera, Kota and Nagashima, Yoshiki and Mannen, Kazuto and Hosouchi, Tsutomu and Shinpo, Sayaka and Kawashima, Moeka and Kotake, Yuki and Yamada, Hiroki and Saga, Yusuke and Otaka, Junnosuke and Araya, Hiroshi and Kotera, Masaaki and Suzuki, Hideyuki and Kushiro, Tetsuo
The Journal of biological chemistry, ISSN 0021-9258, 12/2019, Volume 294, Issue 49, pp. 18662 - 18673
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Hydroxylation | Protein Isoforms | Cytochrome P-450 Enzyme System - metabolism | Plant Proteins - metabolism | Software | Triterpenes - metabolism | Momordica - chemistry | Index Medicus | terpenoid | multifunctional enzyme | secondary metabolism | biosynthesis | plant | Momordica charantia | enzyme catalysis | allylic hydroxylation | cytochrome P450 | Enzymology | cucurbitacin
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33. Full Text Umpolung of Carbonyl Groups as Alkyl Organometallic Reagent Surrogates for Palladium‐Catalyzed Allylic Alkylation
by Zhu, Dianhu and Lv, Leiyang and Li, Chen‐Chen and Ung, Sosthene and Gao, Jian and Li, Chao‐Jun
Angewandte Chemie (International ed.), ISSN 1433-7851, 12/2018, Volume 57, Issue 50, pp. 16520 - 16524
palladium | heterogeneous catalysis | hydrazones | synthetic methods | allylic compounds | Heterogeneous catalysis | Chemotherapy | Ketones | Chemical tests and reagents | Palladium | Aldehydes | Cancer | Carbonyl compounds | Hydrazones | Chemical reactions | Alkylation | Carbonyl groups | Aromatic compounds | Reagents | Catalysis | Nucleophiles | Allyl compounds | Carbonyls
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