The Jia Group

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61. Total Synthesis of (-)-Glaucocalyxin A, Jiuzhou Guo, Bo Li, Weihao Ma, Mallesham Pitchakuntla, Yanxing Jia, Angew. Chem. Int. Ed. 2020, 59, 1 – 5 Link
61. Total Synthesis of (-)-Glaucocalyxin A, Jiuzhou Guo, Bo Li, Weihao Ma, Mallesham Pitchakuntla, Yanxing Jia, Angew. Chem. Int. Ed. 2020, 59, 1 – 5
60. Y. Wang, K. Liu, Z. Yu, Y. Jia. Type-II Pauson-Khand reaction of 1,8-enyne in the attempt of building 7/5 ring of (-)-caribenol A and DFT understanding. Tetrahedron Lett. 2019,... Link
60. Y. Wang, K. Liu, Z. Yu, Y. Jia. Type-II Pauson-Khand reaction of 1,8-enyne in the attempt of building 7/5 ring of (-)-caribenol A and DFT understanding. Tetrahedron Lett. 2019, 60(36), 151001
59. Shibin Shi, Kuo Yuan, Yanxing Jia. Seven-step total synthesis of α-cyclopiazonic acid. Chin. Chem. Lett. 2019, https://doi.org/10.1016/j.cclet.2019.06.048 Link
59. Shibin Shi, Kuo Yuan, Yanxing Jia. Seven-step total synthesis of α-cyclopiazonic acid. Chin. Chem. Lett. 2019, https://doi.org/10.1016/j.cclet.2019.06.048
58. Xiwu Zhang, Xinxian Cai, Bin Huang, Lei Guo, Zhongrun Gao, Prof. Yanxing Jia. Enantioselective Total Syntheses of Pallambins A–D. Angew. Chem. Int. Ed. 2019, 58, 13380 –13384 Link
58. Xiwu Zhang, Xinxian Cai, Bin Huang, Lei Guo, Zhongrun Gao, Prof. Yanxing Jia. Enantioselective Total Syntheses of Pallambins A–D. Angew. Chem. Int. Ed. 2019, 58, 13380 –13384
57. Weihao Ma, Zhi Huang, Yanxing Jia*. Improved synthesis of key intermediate of grayanotoxin III[J]. Chin. J. Org. Chem., 2019, 28(6): 402-407. Link
57. Weihao Ma, Zhi Huang, Yanxing Jia*. Improved synthesis of key intermediate of grayanotoxin III[J]. Chin. J. Org. Chem., 2019, 28(6): 402-407.
56. H. Liu, L. Chen, K. Yuan, Y. Jia, A Ten‐Step Total Synthesis of Speradine C, Angew. Chem. Int. Ed. 2019, 58, 6362. Link
56. H. Liu, L. Chen, K. Yuan, Y. Jia, A Ten‐Step Total Synthesis of Speradine C, Angew. Chem. Int. Ed. 2019, 58, 6362.
55. L. Li, K. Yuan, Q. Jia, Y. Jia, Eight‐Step Total Synthesis of Phalarine by Bioinspired Oxidative Coupling of Indole and Phenol, Angew. Chem. Int. Ed. 2019, 58, 6074. Link
55. L. Li, K. Yuan, Q. Jia, Y. Jia, Eight‐Step Total Synthesis of Phalarine by Bioinspired Oxidative Coupling of Indole and Phenol, Angew. Chem. Int. Ed. 2019, 58, 6074.
54. Zhuang Chen, Mallesham Pitchakuntla and Yanxing Jia. Synthetic approaches to natural products containing 2,3-dihydrobenzofuran skeleton. Nat. Prod. Rep., 2019, 36, 666–690. Link
54. Zhuang Chen, Mallesham Pitchakuntla and Yanxing Jia. Synthetic approaches to natural products containing 2,3-dihydrobenzofuran skeleton. Nat. Prod. Rep., 2019, 36, 666–690.
53. Yuan Kuo, Jia Yanxing. Recent Progress in the Synthesis of 3,4-Fused Indole Alkaloids[J]. Chin. J. Org. Chem., 2018, 38(9): 2386-2399. Link
53. Yuan Kuo, Jia Yanxing. Recent Progress in the Synthesis of 3,4-Fused Indole Alkaloids[J]. Chin. J. Org. Chem., 2018, 38(9): 2386-2399.
52. Lei Li, Zhuang Chen, Xiwu Zhang, and Yanxing Jia. Divergent Strategy in Natural Product Total Synthesis. Chemical Reviews, 2018, 118 (7), pp 3752–3832 Link
52. Lei Li, Zhuang Chen, Xiwu Zhang, and Yanxing Jia. Divergent Strategy in Natural Product Total Synthesis. Chemical Reviews, 2018, 118 (7), pp 3752–3832
51. Lv, J.; Wang, B.; Yuan, K.; Wang, Y.; Jia, Y., Regioselective Direct C‑4 Functionalization of Indole: Total Syntheses of (−)-Agroclavine and (−)-Elymoclavine. Org. Lett. 2017, ... Link
51. Lv, J.; Wang, B.; Yuan, K.; Wang, Y.; Jia, Y., Regioselective Direct C‑4 Functionalization of Indole: Total Syntheses of (−)-Agroclavine and (−)-Elymoclavine. Org. Lett. 2017, 19, (13), 3664−3667.
50. Ma, Y; Jia, Y. J. Synthetic study toward the total synthesis of fumigaclavines A–D. Chin. Pharm. Sci. 2017, 26, (7), 496–503. Link
50. Ma, Y; Jia, Y. J. Synthetic study toward the total synthesis of fumigaclavines A–D. Chin. Pharm. Sci. 2017, 26, (7), 496–503.
49. Liu, H.; Zhang, X.; Shan, D.; Pitchakuntla, M.; Ma, Y.; Jia, Y. Org. Lett. 2017, 19, 3323−3326. Link
49. Liu, H.; Zhang, X.; Shan, D.; Pitchakuntla, M.; Ma, Y.; Jia, Y. Org. Lett. 2017, 19, 3323−3326.
48. Shi, L.; Li, L.; Wang, J.; Huang, B.; Zeng, K.; Jin, H. Zhang, Q.; Jia, Y., Total synthesis of natural spiro-trisindole enantiomers similisines A, B and their stereoisomers.Tet... Link
48. Shi, L.; Li, L.; Wang, J.; Huang, B.; Zeng, K.; Jin, H. Zhang, Q.; Jia, Y., Total synthesis of natural spiro-trisindole enantiomers similisines A, B and their stereoisomers.Tetrahedron Lett. 2017, 58, (20), 1934–1938.
47. Li, L.; Aibibula, P.; Jia, Q.; Jia, Y., Total Syntheses of Naucleamides A−C and E, Geissoschizine, Geissoschizol, (E)‑Isositsirikine, and 16-epi-(E)‑Isositsirikine. Org. Lett.... Link
47. Li, L.; Aibibula, P.; Jia, Q.; Jia, Y., Total Syntheses of Naucleamides A−C and E, Geissoschizine, Geissoschizol, (E)‑Isositsirikine, and 16-epi-(E)‑Isositsirikine. Org. Lett. 2017, 19, (10), 2642−2645.
46. Liu, H.; Jia, Y., Ergot alkaloids: synthetic approaches to lysergic acid and clavine alkaloids. Nat. Prod. Rep. 2017, 34, 411-432. Link
46. Liu, H.; Jia, Y., Ergot alkaloids: synthetic approaches to lysergic acid and clavine alkaloids. Nat. Prod. Rep. 2017, 34, 411-432.
45. Huang, Z.; Lv, J.; Jia, Y., A Simple and Efficient Synthesis of Secondary Alkylamines from Nitroalkanes. ChemistrySelect 2016, 1, (18), 5892–5894. Link
45. Huang, Z.; Lv, J.; Jia, Y., A Simple and Efficient Synthesis of Secondary Alkylamines from Nitroalkanes. ChemistrySelect 2016, 1, (18), 5892–5894.
44. Tao, P.; Jia, Y., C–H bond activation in the total syntheses of natural products. Sci China Chem. 2016, 59, (9), 1109-1125. Link
44. Tao, P.; Jia, Y., C–H bond activation in the total syntheses of natural products. Sci China Chem. 2016, 59, (9), 1109-1125.
43. Tao, P.; Chen, Z.; Jia, Y., A concise gram-scale synthesis of ht-13-A via a rhodium-catalyzed intramolecular C–H activation reaction. Chem. Commun. 2016, 52, (75), 11300--11303... Link
43. Tao, P.; Chen, Z.; Jia, Y., A concise gram-scale synthesis of ht-13-A via a rhodium-catalyzed intramolecular C–H activation reaction. Chem. Commun. 2016, 52, (75), 11300--11303.
42. Aibibula, P.; Huang, Z.; Jia, Y., Asymmetric total synthesis of 3-epi-naucleamide A. J. Chin. Pharm. Sci. 2016, 25, (1), 30-36. Link
42. Aibibula, P.; Huang, Z.; Jia, Y., Asymmetric total synthesis of 3-epi-naucleamide A. J. Chin. Pharm. Sci. 2016, 25, (1), 30-36.
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