SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Corey M. Reeves, Douglas C. Behenna, Brian M. Stoltz, Development of (Trimethylsilyl)ethyl Ester Protected Enolates and Applications in Palladium-Catalyzed Enantioselective Allylic Alkylation: Intermolecular Cross-Coupling of Functionalized Electrophiles, Organic Letters, 2014, 16, 9, 2314

    CrossRef

  2. 2
    Jing Zeng, Yu Jia Tan, Jimei Ma, Min Li Leow, Davin Tirtorahardjo, Xue-Wei Liu, Facile Access to cis-2,6-Disubstituted Tetrahydropyrans by Palladium-Catalyzed Decarboxylative Allylation: Total Syntheses of (±)-Centrolobine and (+)-Decytospolides A and B, Chemistry - A European Journal, 2014, 20, 2
  3. 3
    Nathan B. Bennett, Brian M. Stoltz, A Unified Approach to the Daucane and Sphenolobane Bicyclo[5.3.0]decane Core: Enantioselective Total Syntheses of Daucene, Daucenal, Epoxydaucenal B, and 14-para-Anisoyloxydauc-4,8-diene, Chemistry - A European Journal, 2013, 19, 52
  4. 4
    Peng Zhang, Christian Wolf, Catalytic Enantioselective Difluoroalkylation of Aldehydes, Angewandte Chemie International Edition, 2013, 52, 30
  5. 5
    Zeqian Li, Shaoxiong Zhang, Shoutao Wu, Xiaolei Shen, Liwei Zou, Fengqun Wang, Xiang Li, Fangzhi Peng, Hongbin Zhang, Zhihui Shao, Enantioselective Palladium-Catalyzed Decarboxylative Allylation of Carbazolones: Total Synthesis of (−)-Aspidospermidine and (+)-Kopsihainanine A, Angewandte Chemie, 2013, 125, 15
  6. 6
    Zeqian Li, Shaoxiong Zhang, Shoutao Wu, Xiaolei Shen, Liwei Zou, Fengqun Wang, Xiang Li, Fangzhi Peng, Hongbin Zhang, Zhihui Shao, Enantioselective Palladium-Catalyzed Decarboxylative Allylation of Carbazolones: Total Synthesis of (−)-Aspidospermidine and (+)-Kopsihainanine A, Angewandte Chemie International Edition, 2013, 52, 15
  7. 7
    Nathan B. Bennett, Douglas C. Duquette, Jimin Kim, Wen-Bo Liu, Alexander N. Marziale, Douglas C. Behenna, Scott C. Virgil, Brian M. Stoltz, Expanding Insight into Asymmetric Palladium-Catalyzed Allylic Alkylation of N-Heterocyclic Molecules and Cyclic Ketones, Chemistry - A European Journal, 2013, 19, 14
  8. 8
    Peng Zhang, Christian Wolf, Katalytische enantioselektive Difluoralkylierung von Aldehyden, Angewandte Chemie, 2013, 125, 30
  9. 9
    Fei Pan, Zhi-Quan Lei, Hui Wang, Hu Li, Jian Sun, Zhang-Jie Shi, Rhodium(I)-Catalyzed Redox-Economic Cross-Coupling of Carboxylic Acids with Arenes Directed by N-Containing Groups, Angewandte Chemie, 2013, 125, 7
  10. 10
    Fei Pan, Zhi-Quan Lei, Hui Wang, Hu Li, Jian Sun, Zhang-Jie Shi, Rhodium(I)-Catalyzed Redox-Economic Cross-Coupling of Carboxylic Acids with Arenes Directed by N-Containing Groups, Angewandte Chemie International Edition, 2013, 52, 7
  11. 11
    Jing Zeng, Jimei Ma, Shaohua Xiang, Shuting Cai, Xue-Wei Liu, Stereoselective β-C-Glycosylation by a Palladium-Catalyzed Decarboxylative Allylation: Formal Synthesis of Aspergillide A, Angewandte Chemie, 2013, 125, 19
  12. 12
    Jing Zeng, Jimei Ma, Shaohua Xiang, Shuting Cai, Xue-Wei Liu, Stereoselective β-C-Glycosylation by a Palladium-Catalyzed Decarboxylative Allylation: Formal Synthesis of Aspergillide A, Angewandte Chemie International Edition, 2013, 52, 19
  13. 13
    Shaohua Xiang, Zhiqiang Lu, Jingxi He, Kim Le MaiHoang, Jing Zeng, Xue-Wei Liu, β-Type Glycosidic Bond Formation by Palladium-Catalyzed Decarboxylative Allylation, Chemistry - A European Journal, 2013, 19, 42
  14. 14
    Peng Hu, Yaping Shang, Weiping Su, A General Pd-Catalyzed Decarboxylative Cross-Coupling Reaction between Aryl Carboxylic Acids: Synthesis of Biaryl Compounds, Angewandte Chemie International Edition, 2012, 51, 24
  15. 15
    Peng Hu, Yaping Shang, Weiping Su, A General Pd-Catalyzed Decarboxylative Cross-Coupling Reaction between Aryl Carboxylic Acids: Synthesis of Biaryl Compounds, Angewandte Chemie, 2012, 124, 24
  16. 16
    Peng Hu, Min Zhang, Xiaoming Jie, Weiping Su, Palladium-Catalyzed Decarboxylative C[BOND]H Bond Arylation of Thiophenes, Angewandte Chemie International Edition, 2012, 51, 1
  17. 17
    Peng Hu, Min Zhang, Xiaoming Jie, Weiping Su, Palladium-Catalyzed Decarboxylative C[BOND]H Bond Arylation of Thiophenes, Angewandte Chemie, 2012, 124, 1
  18. 18
    Linglin Wu, Laura Falivene, Emma Drinkel, Sharday Grant, Anthony Linden, Luigi Cavallo, Reto Dorta, Synthesis of 3-Fluoro-3-aryl Oxindoles: Direct Enantioselective α Arylation of Amides, Angewandte Chemie International Edition, 2012, 51, 12
  19. 19
    Linglin Wu, Laura Falivene, Emma Drinkel, Sharday Grant, Anthony Linden, Luigi Cavallo, Reto Dorta, Synthesis of 3-Fluoro-3-aryl Oxindoles: Direct Enantioselective α Arylation of Amides, Angewandte Chemie, 2012, 124, 12
  20. 20
    Norio Shibata, Satoru Suzuki, Tatsuya Furukawa, Hiroyuki Kawai, Etsuko Tokunaga, Zhe Yuan, Dominique Cahard, Construction of Trifluoromethyl-Bearing Quaternary Carbon Centers by Intramolecular Decarboxylative Allylation of α-Trifluoromethyl β-Keto Esters, Advanced Synthesis & Catalysis, 2011, 353, 11-12
  21. 21
    Douglas C. Behenna, Justin T. Mohr, Nathaniel H. Sherden, Smaranda C. Marinescu, Andrew M. Harned, Kousuke Tani, Masaki Seto, Sandy Ma, Zoltán Novák, Michael R. Krout, Ryan M. McFadden, Jennifer L. Roizen, John A. Enquist, David E. White, Samantha R. Levine, Krastina V. Petrova, Akihiko Iwashita, Scott C. Virgil, Brian M. Stoltz, Enantioselective Decarboxylative Alkylation Reactions: Catalyst Development, Substrate Scope, and Mechanistic Studies, Chemistry - A European Journal, 2011, 17, 50
  22. 22
    Andreas Stumpf, Mark Reynolds, Daniel Sutherlin, Srinivasan Babu, Erhard Bappert, Felix Spindler, Michael Welch, John Gaudino, Kilogram-Scale Asymmetric Ruthenium-Catalyzed Hydrogenation of a Tetrasubstituted Fluoroenamide, Advanced Synthesis & Catalysis, 2011, 353, 18
  23. 23
    Ranjan Jana, James J. Partridge, Jon A. Tunge, Migratory Decarboxylative Coupling of Coumarins: Synthetic and Mechanistic Aspects, Angewandte Chemie International Edition, 2011, 50, 22
  24. 24
    Ranjan Jana, James J. Partridge, Jon A. Tunge, Migratory Decarboxylative Coupling of Coumarins: Synthetic and Mechanistic Aspects, Angewandte Chemie, 2011, 123, 22
  25. 25
    Chih-Ming Chou, Indranil Chatterjee, Armido Studer, Stereospecific Palladium-Catalyzed Decarboxylative C(sp3)[BOND]C(sp2) Coupling of 2,5-Cyclohexadiene-1-carboxylic Acid Derivatives with Aryl Iodides, Angewandte Chemie International Edition, 2011, 50, 37
  26. 26
    Joshua J. Day, Ryan M. McFadden, Scott C. Virgil, Helene Kolding, Jennifer L. Alleva, Brian M. Stoltz, The Catalytic Enantioselective Total Synthesis of (+)-Liphagal, Angewandte Chemie, 2011, 123, 30
  27. 27
    Joshua J. Day, Ryan M. McFadden, Scott C. Virgil, Helene Kolding, Jennifer L. Alleva, Brian M. Stoltz, The Catalytic Enantioselective Total Synthesis of (+)-Liphagal, Angewandte Chemie International Edition, 2011, 50, 30
  28. 28
    Weibo Wang, Jacek Jasinski, Gerald B. Hammond, Bo Xu, Fluorine-Enabled Cationic Gold Catalysis: Functionalized Hydration of Alkynes, Angewandte Chemie International Edition, 2010, 49, 40
  29. 29
    Weibo Wang, Jacek Jasinski, Gerald B. Hammond, Bo Xu, Fluorine-Enabled Cationic Gold Catalysis: Functionalized Hydration of Alkynes, Angewandte Chemie, 2010, 122, 40
  30. 30
    Xiao Han, Fangrui Zhong, Yixin Lu, Highly Enantioselective Amination Reactions of Fluorinated Keto Esters Catalyzed by Novel Chiral Guanidines Derived from Cinchona Alkaloids, Advanced Synthesis & Catalysis, 2010, 352, 16
  31. 31
    Xiao Han, Jacek Kwiatkowski, Feng Xue, Kuo-Wei Huang, Yixin Lu, Asymmetric Mannich Reaction of Fluorinated Ketoesters with a Tryptophan-Derived Bifunctional Thiourea Catalyst, Angewandte Chemie, 2009, 121, 41
  32. 32
    Xiao Han, Jacek Kwiatkowski, Feng Xue, Kuo-Wei Huang, Yixin Lu, Asymmetric Mannich Reaction of Fluorinated Ketoesters with a Tryptophan-Derived Bifunctional Thiourea Catalyst, Angewandte Chemie International Edition, 2009, 48, 41
  33. 33
    Hai-Feng Wang, Hai-Feng Cui, Zhuo Chai, Peng Li, Chang-Wu Zheng, Ying-Quan Yang, Gang Zhao, Asymmetric Synthesis of Fluorinated Flavanone Derivatives by an Organocatalytic Tandem Intramolecular Oxa-Michael Addition/Electrophilic Fluorination Reaction by Using Bifunctional Cinchona Alkaloids, Chemistry - A European Journal, 2009, 15, 48
  34. 34
    Hyunseok Kim, Phil Ho Lee, Palladium-Catalyzed Decarboxylative sp-sp2 Cross-Coupling Reactions of Aryl and Vinyl Halides and Triflates with α,β-Ynoic Acids using Silver Oxide, Advanced Synthesis & Catalysis, 2009, 351, 17
  35. 35
    Zhiyong Jiang, Yuanhang Pan, Yujun Zhao, Ting Ma, Richmond Lee, Yuanyong Yang, Kuo-Wei Huang, Ming Wah Wong, Choon-Hong Tan, Synthesis of a Chiral Quaternary Carbon Center Bearing a Fluorine Atom: Enantio- and Diastereoselective Guanidine-Catalyzed Addition of Fluorocarbon Nucleophiles, Angewandte Chemie International Edition, 2009, 48, 20
  36. 36
    Zhiyong Jiang, Yuanhang Pan, Yujun Zhao, Ting Ma, Richmond Lee, Yuanyong Yang, Kuo-Wei Huang, Ming Wah Wong, Choon-Hong Tan, Synthesis of a Chiral Quaternary Carbon Center Bearing a Fluorine Atom: Enantio- and Diastereoselective Guanidine-Catalyzed Addition of Fluorocarbon Nucleophiles, Angewandte Chemie, 2009, 121, 20
  37. 37
    Nathaniel H. Sherden, Douglas C. Behenna, Scott C. Virgil, Brian M. Stoltz, Unusual Allylpalladium Carboxylate Complexes: Identification of the Resting State of Catalytic Enantioselective Decarboxylative Allylic Alkylation Reactions of Ketones, Angewandte Chemie International Edition, 2009, 48, 37
  38. 38
    Nathaniel H. Sherden, Douglas C. Behenna, Scott C. Virgil, Brian M. Stoltz, Unusual Allylpalladium Carboxylate Complexes: Identification of the Resting State of Catalytic Enantioselective Decarboxylative Allylic Alkylation Reactions of Ketones, Angewandte Chemie, 2009, 121, 37
  39. 39
    Vincent A. Brunet, David O'Hagan, Catalytic Asymmetric Fluorination Comes of Age, Angewandte Chemie International Edition, 2008, 47, 7
  40. 40
    Vincent A. Brunet, David O'Hagan, Katalytische asymmetrische Fluorierungen, Angewandte Chemie, 2008, 120, 7
  41. 41
    Zhan Lu, Shengming Ma, Metal-Catalyzed Enantioselective Allylation in Asymmetric Synthesis, Angewandte Chemie International Edition, 2008, 47, 2
  42. 42
    Zhan Lu, Shengming Ma, Metallkatalysierte enantioselektive Allylierungen in der asymmetrischen Synthese, Angewandte Chemie, 2008, 120, 2
  43. 43
    Justin T. Mohr, Brian M. Stoltz, Enantioselective Tsuji Allylations, Chemistry – An Asian Journal, 2007, 2, 12
  44. 44
    Shelli R. Waetzig, Dinesh K. Rayabarapu, Jimmie D. Weaver, Jon A. Tunge, A Versatile Hexadiene Synthesis by Decarboxylative sp3–sp3 Coupling/Cope Rearrangement, Angewandte Chemie International Edition, 2006, 45, 30
  45. 45
    Shelli R. Waetzig, Dinesh K. Rayabarapu, Jimmie D. Weaver, Jon A. Tunge, A Versatile Hexadiene Synthesis by Decarboxylative sp3–sp3 Coupling/Cope Rearrangement, Angewandte Chemie, 2006, 118, 30
  46. 46
    Barry M. Trost, Robert N. Bream, Jiayi Xu, Asymmetric Allylic Alkylation of Cyclic Vinylogous Esters and Thioesters by Pd-Catalyzed Decarboxylation of Enol Carbonate and β-Ketoester Substrates, Angewandte Chemie International Edition, 2006, 45, 19
  47. 47
    Barry M. Trost, Robert N. Bream, Jiayi Xu, Asymmetric Allylic Alkylation of Cyclic Vinylogous Esters and Thioesters by Pd-Catalyzed Decarboxylation of Enol Carbonate and β-Ketoester Substrates, Angewandte Chemie, 2006, 118, 19
  48. 48
    G. K. Surya Prakash, Petr Beier, Aufbau fluorierter Kohlenstoffstereozentren, Angewandte Chemie, 2006, 118, 14
  49. 49
    G. K. Surya Prakash, Petr Beier, Construction of Asymmetric Fluorinated Carbon Centers, Angewandte Chemie International Edition, 2006, 45, 14
  50. 50
    Shu-Li You, Li-Xin Dai, Enantioselective Palladium-Catalyzed Decarboxylative Allylic Alkylations, Angewandte Chemie International Edition, 2006, 45, 32
  51. 51
    Shu-Li You, Li-Xin Dai, Enantioselektive Palladium-katalysierte decarboxylierende allylische Alkylierungen, Angewandte Chemie, 2006, 118, 32
  52. 52
    Neu im Kuratorium und im Internationalen Beirat, Angewandte Chemie, 2006, 118, 1
  53. 53
    New Members of the Editorial Board and the International Advisory Board, Angewandte Chemie International Edition, 2006, 45, 1