83. Amide C–N bonds activation by A new variant of bifunctional N-heterocyclic carbene

Yuxing Cai, Yuxin Zhao, Kai Tang, Hong Zhang, Xueling Mo, Jiean Chen,* Yong Huang*

Nat. Commun. 2024, 15, 496.

82. Discovery and synthesis of atropisomerically chiral acyl-substituted stable vinyl sulfoxonium ylides

Fengjin Wu, Yichi Zhang, Ruiqi Zhu, Yong Huang*

Nat. Chem. 2024, 16, 132-139.


81. A Carbene Relay Strategy for Cascade Insertion Reactions

Li Li, Chenggang Mi, Guanwang Huang, Meirong Huang, Yuyi Zhu, Shao-Fei Ni, Zhaofeng Wang,* Yong Huang*

Angew. Chem. Int. Ed. 2023, e202312793

80. Enantioselective SN2 Alkylation of Homoenolates by N-Heterocyclic Carbene Catalysis

En Li, Kai Tang, Zhuhui Ren, Xiaoyun Liao, Qianchen Liu, Yong Huang,* Jiean Chen*

Adv. Sci. 2023, 2303517

79. Incorporating Domain Knowledge and Structure-Based Descriptors for Machine Learning: A Case Study of Pd-Catalyzed Sonogashira Reactions

Kalok Chan, Long Thanh Ta, Yong Huang,* Haibin Su,* Zhenyang Lin*

Molecules 2023, 28, 4730


78. Photoredox Cleavage of a Csp3–Csp3 Bond in Aromatic Hydrocarbons

Ke Liao, Cho Ying Chan, Siqi Liu, Xinhao Zhang, Jiean Chen*, Yong Huang*

J. Am. Chem. Soc. 2023, 145, 12284–12292

77. Recent Advances in Ynenamine Chemistry

BingyangHan, ZhaofengWang,* YongHuang*

Chem. Rec. 2023, 23, e202300099 (Invited Account)


76. Hierarchical graph learning for protein–protein interaction

Ziqi Gao, Chenran Jiang, Jiawen Zhang, Xiaosen Jiang, Lanqing Li, Peilin Zhao, Huanming Yang, Yong Huang,* Jia Li*

Nat. Commun. 2023, 14, 1093.


75. Synthesis of I(III)/S(VI) reagents and their reactivity in photochemical cycloaddition reactions with unsaturated bonds

Li Li, Kun Deng, Yajie Xing, Cheng Ma, Shao-Fei Ni, Zhaofeng Wang,* Yong Huang* Nat. Commun. 2022, 13, 6588.

74. A Thioether-Catalyzed Cross-Coupling Reaction of Allyl Halides and Arylboronic Acids

Jingwei Xu, Zhiqi He, Jiwei Zhang, Jiean Chen,* Yong Huang* Angew. Chem. Int. Ed. 2022, 61, e202211408.


73. An NHC-catalyzed [3+2] cyclization of β-disubstituted enals with benzoyl cyanides

Wangsheng Liu, Linrui Zhang, Xiaoyun Liao, Jiean Chen,* Yong Huang* Chem. Commun. 2022, 58, 9742-9745.


72. Catalytic cleavage and functionalization of bulky and inert Csp3–Csp3 bonds via a relayed proton-coupled electron transfer strategy

Ke Liao, Fengjin Wu, Jiean Chen,* Yong Huang* Cell Rep. Phys. Sci. 2022, 3, 100763.

71. Enantioselective Seleno-Michael Addition Reactions Catalyzed by a Chiral Bifunctional N-Heterocyclic Carbene with Noncovalent Activation

En Li, Jiean Chen,* Yong Huang*  Angew. Chem. Int. Ed. 2022, 61, e202202040.


70. Enantioselective synthesis of acyclic monohydrosilanes by steric hindrance assisted C-H silylation

Delong Mu, Shuqiong Pan, Xiaoyu Wang, Xiaoyun Liao, Yong Huang*, Jiean Chen*  Chem. Commun. 2022, 58, 7388-7391.

69.  N-Heterocyclic Carbene-Catalyzed 1,4-Alkylcylation of 1,3-Enynes 

Yuxing Cai, Jiean Chen,*  and Yong Huang.*  Org. Lett. 2021, 23, 9251-9255.

68. A cross-coupling Reaction between Aliphatic Aldehydes and Sulfonium Salts

Baoli Chen, Li Li,  Jiean Chen,*  and Yong Huang.*  Adv. Synth. Catal. 2022, 364, 30-34.

 

67. N‑Heterocyclic Carbene-Catalyzed Four-Component Reaction: Chemoselective Cradical-Cradical Relay Coupling Involving the Homoenolate Intermediate

Zhen Li, Meirong Huang, Xinhao Zhang, Jiean Chen,*  and Yong Huang.*  ACS catal. 2021, 11, 10123-10130.  

66. Synthesis of a-chiral phosphine sufides via no-covalent organocatalysis

En Li, Qian Wang, Yuxing Cai, Jiean Chen,*  and Yong Huang.*  Cell Reports Physical Science. doi:rg/10.1016/j.xcrp.2021.10.

65. A Bifunctional N‑Heterocyclic Carbene as a Noncovalent Organocatalyst for Enantioselective Aza-Michael Addition Reactions

Fangfang Guo, Jiean Chen,* and Yong Huang.* ACS catal. 2021, 11, 6316-6324.  

64. Photo-induced energy transfer relay of N-heterocyclic carbene catalysis: an asymmetric a-fluorination/isomerization cascade

Xinhang Jiang, En Li, Jiean Chen,* and Yong Huang.*  Chem. Commun., 2021, 57, 729-732.

63. MolecularInsightsintoSmall-MoleculeDrugDiscovery forSARS-CoV-2

Hailei Su, Feng Zhou, Ziru Huang, Xiaohua Ma, Kathiresan Natarajan, Minchuan Zhang, Yong Huang,* and Haibin Su.*  Angew. Chem. Int. Ed. 2021, 60, 9789–9802.

image

62. Enantioselective Intramolecular [2,3]-Sigmatropic Rearrangement of Aldehydes via a Sulfonium Enamine Intermediate

Li Li, Baoli Chen, Jiean Chen,* Yong Huang.* Angew. Chem. Int. Ed. 2020, 59, 20904 –20908.

61. Direct Synthesis of Bicyclic Acetals via Visible Light Catalysis

Fengjin Wu, Leifeng Wang, Ying Ji, Ge ou, Hong Shen, David A. Nicewicz,* Jiean Chen,* Yong Huang.*  iScience 2020, 23, 10139.


60. Ligand-Controlled C-O Bond Coupling of Carboxylic Acids and Aryl Iodides: Experimental and Computational Insights

Li Li, Feifei Song, Xiumei Zhong, Yun-Dong Wu, Xinhao Zhang,* Jiean Chen,* and Yong Huang.* Adv. Synth. Catal. 2020, 362, 126 – 132

59. Alcohol-Directed ortho-C–H Alkenylation

Li Li, Qinglan Liu, Jiean Chen *, Yong Huang *. Synlett 2019, 30, A-E. DOI: 10.1055/s-0037-1611538

58. Enantio- and Diastereoselective Hydrofluorination of Enals via N-Heterocyclic Carbene Catalysis

Leming Wang, Xinhang Jiang, Jiean Chen,* Yong Huang*. Angew. Chem. Int. Ed. 2019. DOI:10.1002/anie.201902989

57. N‐Heterocyclic Carbenes as Brønsted Base Catalysts

Jiean Chen, Yong Huang. Book Author(s): Akkattu T. Biju. DOI :10.1002/9783527809042.ch9

56. Dehydrogenative Annulation of γ,δ-Unsaturated Amides and Alkynes via Double C-H Activation

Wang Zhen, Li En, He Zhiqi, Chen Jiean, Huang Yong. Acta Phys. -Chim. Sin. 2019, 35, 0001–0009. DOI: 10.3866/PKU.WHXB201811038.

55.Switching Reaction Pathways by Cooperative Catalysis of N-Heterocyclic Carbene and Lewis Acids

Wang Leming, Wang Qian, Chen Jiean*, Huang Yong*. Acta Chim. Sinica 2018, 76, 850—856.

54. Structure-Based Drug Design and Identification of H2O‑Soluble and Low Toxic Hexacyclic Camptothecin Derivatives with Improved Efficacy in Cancer and Lethal Inflammation Models in Vivo
Peichen Pan,† Jiean Chen,§ Xijian Li,§ Miyang Li,§ Huidong Yu,∥ Jean J. Zhao,⊥,# Jing Ni,⊥,#Xuwen Wang,† Huiyong Sun,† Sheng Tian,∇ Feng Zhu,† Feng Liu,∇ Yong Huang,*,§ and Tingjun Hou*,†,‡  J. Med. Chem. 2018, XXX, XXX−XXX. DOI: 10.1021/acs.jmedchem.8b00498

53. Aerobic Oxidation/Annulation Cascades via Synergistic Catalysis of RuCl3 and N‐Heterocyclic Carbenes

Qian Wang,  Jiean Chen*,  Yong Huang*.  Chem. Eur. J. 2018, 24, 12806 – 12810. DOI: 10.1002/chem.201803254 

52. Enantioselective hydroamidation of enals by trapping of a transient acyl species

Pengfei Yuan, Jiean Chen*, Jing Zhao*, Yong Huang*. Angew. Chem. Int. Ed. 2018. 57, 8503 –8507. DOI: 10.1002/anie.201803556

51. A Transition-Metal-Free Suzuki-Type Cross-Coupling Reaction of Benzyl Halides and Boronic Acids via 1,2-Metallate Shift

Zhiqi He, Feifei Song, Huan Sun, and Yong Huang*. J. Am. Chem. Soc. 2018, 140, 2693-2699. DOI: 10.1021/jacs.8b00380

50. Streamlined asymmetric α-difunctionalization of ynones

Siyu Peng1, Zhaofeng Wang1, Linxing Zhang, Xinhao Zhang* & Yong Huang*. Nat. Commun. 2018, 9, 375. DOI: 10.1038/s41467-017-02801-9

49. Enantioselective Cooperative Proton-Transfer Catalysis using Chiral Ammonium Phosphates

Linrui Zhang, Pengfei Yuan, Jiean Chen* and Yong Huang*. Chem. Commun., 2018, 54, 1473. DOI: 10.1039/C7CC09549J

48. Direct Synthesis of Polysubstituted Aldehydes via Visible-Light-Catalysis

Fengjin Wu1, Leifeng Wang1, Jiean Chen*, David A. Nicewicz*, Yong Huang*. Angew. Chem. Int. Ed. 2018, 57, 2174-2178. DOI: 10.1002/anie.201712384

47. Iridium-Catalyzed Aerobic α,β-Dehydrogenation of γ,δ-Unsaturated Amides and Acids: Activation of Both α- and β-C–H bonds through an Allyl–Iridium Intermediate

Zhen Wang1, Zhiqi He1, Linrui Zhang and Yong Huang*, J. Am. Chem. Soc., 2018, 140, 735−740. DOI: 10.1021/jacs.7b11351

46. Amine-Triggered 6p-Electrocyclization–Aromatization Cascade of Ynedienamines

Xijian Li, Huidong Yu, and Yong Huang*, Adv. Synth. Catal. 2017, 359, 1379 – 1387

45. Combating Drug-Resistant Mutants of Anaplastic Lymphoma Kinase with Potent and Selective Type‑I 1/2 Inhibitors by Stabilizing Unique DFG-Shifted Loop Conformation

Peichen Pan, Huidong Yu, Qinglan Liu, et al. Yong Huang*, and Tingjun Hou*, ACS Cent. Sci. 2017, DOI: 10.1021/acscentsci.7b00419

 

44. Construction of Pyridazine Analogues via Rhodium-mediated C-H Activation

Chao Yang, Feifei Song, Jiean Chen*, and Yong Huang*, Adv. Synth. Catal. 2017, 359, 3496-3502.

43. Enantioselective β‑Protonation of Enals via a Shuttling Strategy

Jiean Chen1, Pengfei Yuan1, Leming Wang, and Yong Huang*, J. Am. Chem. Soc. 2017, 139, 7045−7051.

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42. Visible Light Mediated [4+2] Cycloaddition of Styrenes Synthesis of Tetralin Derivatives

Leifeng Wang, Fengjin Wu, Jiean Chen, David A. Nicewicz,* and Yong Huang*,  Angew. Chem. Int. Ed. 2017, 56, 6896-6900.

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41.Synthesis of Optically Active Oxazolines by an Organocatalytic Isocyanoacetate Aldol Reaction with α-Keto Esters

Fei Wang, Jiean Chen* and Yong Huang*, Synlett 2017,28, 1300-1304. （Invited Synlett Cluster）

Oxazolines

 

40. A Migratory Ether Formation Route to Medium-Sized Sugar Mimetics

Hao Jiang, Li-Ping Xu, Yan Fang, Zhen-Xing Zhang, Zhen Yang,* and Yong Huang*, Angew. Chem. Int. Ed., 2016, 55, 14340 –14344.

TOC-2016-12-4-JH

39. Diverting C−H Annulation Pathways Nickel-Catalyzed Dehydrogenative Homologation of Aromatic Amides

Zhiqi He and Yong Huang*,  ACS Catal. 2016, 6, 7814−7823.

TOC

38. Advances in the development of catalytic tethering directing groups for C–H functionalization reactions

Huan Sun, Nicolas Guimond* and Yong Huang*, Org. Biomol. Chem., 2016,14, 8389–8397.（Invited Perspective）

 

37. Ligand-Assisted Palladium(II)/(IV) Oxidation for sp3 C-H Fluorination

Huan Sun, Yi Zhang, Ping Chen, Yun-Dong Wu*, Xinhao Zhang* and Yong Huang*,  Adv. Synth. Catal., 2016, 358, 1946.（Very Important Paper, Front Cover）

TOC_看图王

36. New frontiers of N-heterocyclic carbene catalysis

Jiean Chen and Yong Huang*, Sci. China Chem., 2016, 59, 251(Invited Perspective)

45 abstract

 

35. Asymmetric Sulfa-Michael Addition of α,β-Unsaturated Esters/Amides Using a Chiral N-Heterocyclic Carbene as a Noncovalent Organocatalyst

Pengfei Yuan, Sixuan Meng, Jiean Chen* and Yong Huang*, Synlett, 2016, 27, 1068.（Invited Synlett Cluster）

46-2

34. Recent Progress in the Development of Multitasking Directing Groups for Carbon-Hydrogen Activation Reactions

Huan Sun and Yong Huang*, Synlett. 2015, 26, 2751. (Invited Account)

123-1

33. Highly Enantioselective Aza-Michael Reaction between Alkyl Amines and β-Trifluoromethyl β-Aryl Nitroolefins

Leming Wang, Jiean Chen and Yong Huang*, Angew. Chem. Int. Ed. 2015, 54, 15414.

43

32. Asymmetric intramolecular α-cyclopropanation of aldehydes using a donor/acceptor carbene mimetic

Chaosheng Luo, Zhen Wang and Yong Huang*, Nature Commun. 2015, 6, 10041.

42

31. Highly enantioselective sulfa-Michael addition reactions using N-heterocyclic carbene as a noncovalent organocatalyst

Jiean Chen, Sixuan Meng, Leming Wang, Hongmei Tang and Yong Huang*, Chem. Sci. 2015, 6, 4184.

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30. A Copper-Catalyzed Aerobic Domino Process for The Synthesis of Isoindolin-1-ylidene Derivatives

Hu Chen, Qian Wang and Yong Huang*, Tetrahedron 2015, 71, 3632. （Invited Contribution for a Special Issue)

CH

29. Synthesis of Tetrasubstituted 1-silyloxy-3-aminobutadienes and Chemistry Beyond Diels–Alder Reactions

Xijian Li, Siyu Peng, Li Li and Yong Huang*, Nature Commun. 2015, 6, 6913.

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28. Direct Fluorination of Styrenes

Qian Shao, and Yong Huang*, Chem. Commun. 2015, 51, 6584-6586.

sq

 

27. Synthesis of Indolo[2,1-a]isoquinolines via a Triazene-Directed C–H Annulation Cascade

Huan Sun, Chengming Wang, Yun-Fang Yang, Ping Chen, Yun-Dong Wu*, Xinhao Zhang* and Yong Huang*, J. Org. Chem. 2014, 79, 11863-11872.

TOC

 

26. Ruthenium-Catalyzed Redox-Neutral C–H Activation via N–N Cleavage: Synthesis of N-Substituted Indoles

Zhenxing Zhang, Hao Jiang and Yong Huang*, Org. Lett. 2014, 16, 5976–5979.

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25. Directed Arenealkyne Annulation Reactions via Aerobic Copper Catalysis

Yi Zhang, Qian Wang, Huidong Yu* and Yong Huang*, Org. Biomol. Chem. 2014, 12, 8844-8850.

TOC-zy

24. Highly ortho-Selective Trifluoromethylthiolation Reactions using a Ligand Exchange Strategy

Weiyu Yin, Zhaofeng Wang and Yong Huang*, Adv. Synth. Catal. 2014, 356, 2998 – 3006.

TOC-ywy

23. A General Synthesis of Ynones from Aldehydes via Oxidative C–C bond Cleavage under Aerobic Conditions

Zhaofeng Wang, Li Li and Yong Huang*, J. Am. Chem. Soc. 2014, 136, 12233–12236.

TOC

22. A multitasking functional group leads to structural diversity using designer C–H activation reaction cascades

 Ying Chen, Dongqi Wang, Pingping Duan, Rong Ben, Lu Dai, Xiaoru Shao, Mei Hong, Jing Zhao* and Yong Huang*, Nature Commun. 2014, 5, 4610.

TOC

21. Asymmetric catalysis with N-heterocyclic carbenes as non covalent chiral templates

Jiean Chen and Yong Huang*,  Nature Commun. 2014, 5, 3437.

NHC catalysis thumbnail

20. Selective synthesis of indazoles and indoles via triazene–alkyne cyclization switched by different metals

Yan Fang, Chengming Wang, Shengqin Su, Haizhu Yu* and Yong Huang*, Org. Biomol. Chem. 2014,12, 1061-1071.

FY triazene thumbnail

 

c3ob42088d 1061..1071 ++

19. Palladium catalyzed acetoxylation of benzylic C–H bonds using a bidentate picolinamide directing group

Tao Cheng, Weiyu Yin, Yi Zhang, Yingnan Zhang and Yong Huang*, Org. Biomol. Chem. 2014,12, 1405-1411.

 

CT benzylic oxidation thumbnail

 

 18.Direct α-Vinylidenation of Aldehydes and Subsequent Cascade Gold and Amine Catalysts Work Synergistically

 Zhaofeng Wang, Xijian Li, Yong Huang*, Angew. Chem. Int. Ed. 2013, 42, 14219-14223.

TOCWZF-allenylation cover

17.Synthesis of α,β-unsaturated carbonyl compounds via a visible light promoted organocatalytic aerobic oxidation

Junlin Zhang, Leming Wang, Qi Liu, Zhen Yang*, and Yong Huang*, Chem. Commun. 2013, 49, 11662-11664.

ZJL-photo-enone-synthesis-TOC

 

16. Enantioselective synthesis of 1,2,4-triazolines catalyzed by a cinchona alkaloid derived organocatalyst

Qian Shao, Jiean Chen, Meihua Tu, David W. Piotrowski and Yong Huang*, Chem. Commun. 2013, 49, 11098-11100.

SQ-triazene-CC-TOC

15. Traceless Directing Strategy Efficient Synthesis of N-Alkyl Indoles via Redox-Neutral C–H Activation

 Chengming Wang and Yong Huang*, Org. Lett. 2013, 15, 5294-5297.

WCM-Nitroso-Indole-OL-TOC

14. A Highly Diastereo- and Enantioselective Synthesis of Tetrahydroquinolines Quaternary Stereogenic Center Inversion and Functionalization

Chaosheng Luo and Yong Huang*, J. Am. Chem. Soc. 2013, 135, 8193–8196.

Highlighted by SYNFACTS, 2013, 9(8), 0898; DOI-10.1055s-0033-1339442.

LCS-THQ-JACS-TOC

13. General and Efficient Synthesis of Indoles through Triazene Directed C–H Annulation

Chengming Wang, Huan Sun, Yan Fang, and Yong Huang*, Angew. Chem. Int. Ed. 2013, 52, 5795-5798. (cover)

Highlighted by Chinese-Journal-of-Organic-Chemistry-2013-337-1593.

WCM-Triazene-Indole-Angew-TOCWCM-Triazene-Indole-Angew-Cover

12. A Highly Diastereoselective and Enantioselective Synthesis of Polysubstituted Pyrrolidines via an Organocatalytic Dynamic Kinetic Resolution Cascade

Tao Cheng, Sixuan Meng, and Yong Huang*, Org. Lett. 2013, 15 , 1958–1961.

CT-Aza-Henry-OL-TOC

11. Highly Practical Synthesis of Nitriles and Heterocycles from Alcohols under Mild Conditions by Aerobic Double Dehydrogenative Catalysis

Weiyu Yin, Chengming Wang and Yong Huang*, Org. Lett. 2013, 15, 1850–1853.

Highlighted-by-SYNFACTS-2013-97-0722.-DOI_-10.1055_s-0033-1339227., Highlighted by organic chemistry portal

Ywy-OH-to-CN-OL-TOC

10. Highly trans Stereoselective Synthesis of Bicyclic Isoxazolidines via Copper Catalyzed Triple Cascade Catalysis

Hu Chen, Zhaofeng Wang, Yingnan Zhang and Yong Huang*, J. Org. Chem. 2013, 78, 3503-3509.

Highlighted by SYNFACTS, 2013, 9(6), 0602. DOI: 10.1055/s-0033-1338792.

CH-Nitrone-JOC-TOC

9. Computational study on mechanism of-RhIII-catalyzed oxidative Heck coupling of phenol carbamates with alkenes

Qi Zhang, Hai-Zhu Yu, Yi-Tong Li, Lei Liu, Yong Huang* and Yao Fu*, Dalton Trans. 2013, 42, 4175-4184.

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8. Expanding Structural Diversity Removable and Manipulable Directing Groups for C-H Activation

Chengming Wang, Yong Huang*, Synlett. 2013, 24,145.(invited)

WCM-DG-Synpacts-TOC

7. An Air-State Fe3S4 Complex with Properties Similar to Those of the HOXair State of the Diiron Hydrogenases

Yong Huang, Weiming Gao, Torbjõrn Åkermark, Mingrun Li, BjÖrn Åkermark*, Eur. J. Inorg. Chem. 2012, 27, 4259-4263.

Gao-Fe-EJIC-TOC

6.RhodiumIII Catalyzed C-H Activation of Arenes Using a Versatile and Removable Triazene Directing Group

Chengming Wang, Hu Chen, Zhaofeng Wang, Jiean Chen and Yong Huang*, Angew. Chem. Int. Ed. 2012, 51, 7242-7245. (cover)

Highlighted by organic chemistry portal

WCM-Triazene-Heck-Angew-TOCWCM-Triazene-Heck-Angew-Cover

5.One pot synthesis of useful heterocycles in medicinal chemistry using a cascade strategy

Guiyong Wu, Weiyu Yin, Hong C. Shen,* and Yong Huang*, Green. Chem. 2012, 14, 580-585. (cover)

WGY-One-pot-Hetercycles-Green-TOCWGY-One-pot-Hetercycles-Green-cover

4.General palladium catalyzed aerobic dehydrogenation to generate double bonds

Weiming Gao, Zhiqi He, Yong Qian, Jing Zhao* and Yong Huang*, Chem. Sci. 2012, 3, 883-886.

Chem Sci Graphic Abstract

3. A Thiourea-Oxazoline Library with Axial Chirality Ligand Synthesis and Studies of the Palladium-Catalyzed Enantioselective Bismethoxycarbonylation-of-Terminal-Olefins

Ying-Xiang Gao, Le Chang, Hang Shi, Bo Liang, Kittiya Wongkhan, Duangduan Chaiyaveij, Andrei.S. Batsanov, Todd.B. Marder,* Chuang Chuang Li,* Zhen Yang,* Yong Huang* Adv, Synth. Catal. 2010, 352, 1955-1966.

GYX-thiourea-ASC-TOC

2. Enantioselective Organo-Cascade Catalysis

Yong Huang, Abbas M. Walji , Catharine H. Larsen, and David W. C. MacMillan *, J. Am. Chem. Soc. 2005, 127, 15051-15053.

QQ截图20121011145630

1. Hydrogen bonding: Single enantiomers from a chiral-alcohol catalyst

Yong Huang, Aditya K. Unni, Avinash N. Thadani and Viresh H. Rawal*, Nature 2003, 424, 146-146.

TADDOL-TOC

Patents:

1. “A method to Prepare Nitriles” 201210447319.X
2. "Methods of Preparing Ketones and Their Derivatives" 201110252324.0
3. "Preparation of Cyclopropyl Compounds Containing Pyridine and Pyrimidine Rings as GPR119 Receptor Agonists for the Treatment of Type 2 Diabetes and Related Diseases" WO2009129036
4. "Preparation of Bipiperidinyl Compounds as GPR-119 Agonists for Treating and Preventing Diabetes" WO2008085316
5. "Acyl Bipiperidinyl Compounds as G-protein Coupled Receptor GPR-119 Agonists, Their Preparation, Compositions Containing Such Compounds and Methods of Treatment" WO2008076243
6. "Methods of Performing Cycloadditions, Reaction Mixtures, and Methods of
Performing Asymmetric Catalytic Reactions" US 7230125

C

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