305. Tri-insertion with Dearomatization of Terminal Arylalkynes at Carborane Based Frustrated Lewis Pair Template
Zhang, J.; Xie, Z. Chem. Sci. 2020, Ahead of Print. 304. Synthesis and X-ray characterization of 15- and 16-vertex closo-carboranes
Zheng, F.; Yui, T.; Xie, Z. Nat Commun. 2020, Ahead of Print. 303. Transition-Metal-Free Cross-Coupling Reaction of Iodocarboranes with Terminal Alkynes Enabled by UV Light: Synthesis of 1-Alkynyl-o-Carboranes and Carborane-Fused Cyclics
Ni, H.; Lu, Z.; Xie, Z. J. Am. Chem. Soc. 2020, Ahead of Print. 302. Palladium-Catalyzed Oxidative Annulation of 1-Hydroxy-o-Carborane with Internal Alkynes: Facile Synthesis of Carborane-Fused Oxaboroles
Cheng, R.; Qiu, Z.; Xie, Z. Chin. J. Chem. 2020, Ahead of Print. 301. 8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of o-carboranes
Chen Y.; Quan, Y.; Xie, Z. Chem. Comm. 2020, Ahead of Print. 300. Magnesium-mediated sp3 C–H activation in cascade cyclization of 1-arylethynyl-2-alkyl-o-carboranes: efficient synthesis of carborane-fused cyclopentanes
Zhang, J.; Tang, C.; Xie, Z. Chem. Sci. 2020, 11(36), 9925-9929. 299. Palladium-Catalyzed Carbonylative Annulation of 1-Hydroxy-o-Carborane and Internal Alkynes via Regioselective B-H Activation
Au, Y. K.; Quan, Y.; Xie, Z. Chem. Asian J. 2020, 15, 2170-2173. 298. Light-promoted copper-catalyzed cage C-arylation of o-carboranes: facile synthesis of 1-aryl-o-carboranes and o-carborane-fused cyclics
Ni, H.; Lu, Z.; Xie, Z. New J. Chem. 2020, Ahead of Print. 297. [2 + 2] Cycloaddition of o-Carboryne with Vinyl Ethers: Synthesis of Carborane-Fused Cyclobutanes
Zhang, J.; Xie, Z. Organometallics 2020, Ahead of Print. 296. Ir-Catalyzed Selective Dehydrogenative Cross-Coupling of Aryls with o-Carboranes via Mixed Directing-Group Strategy
Chen, Y; Quan, Y.; Xie, Z. Chem. Comm. 2020, 56, 7001-7004. 295. Copper-Catalyzed Electrochemical Selective B–H Oxygenation of o-Carboranes at Room Temperature
Au, Y. K.; Lyu, H.; Quan, Y.; Xie, Z. J. Am. Chem. Soc. 2020, 142, 6940-6945. 294. Iridium-Catalyzed Regioselective B(3)-Alkenylation/B(3,6)-Dialkenylation of o‐Carboranes by Direct B−H Activation
Cheng, R.; Qiu, Z.; Xie, Z. Chem. Eur. J. 2020, 26, 7212-7218 293. One-Pot Process to Carborano-Coumarin via Catalytic Cascade Dehydrogenative Cross-Coupling
Au, Y. K.; Lyu, H.; Quan, Y.; Xie, Z. Chin. J. Chem. 2020, 38, 383-388. 292. Pd-Catalyzed Selective Bifunctionalization of 3-Iodo-o-Carborane by Pd Migration
Ge, Y.; Zhang, J.; Qiu, Z. Xie, Z. Angew. Chem. Int. Ed., 2020, 59, 4851-4855. 291. Palladium- catalyzed intramolecular dehydrogenative coupling of BH and OH: synthesis of carborane- fused benzoxaboroles
Cui, C.; Zhang, J.; Qiu, Z.; Xie, Z. Dalton Trans. 2020, 49, 1380-1383. |
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The contents of the Center of Novel Functional Molecules website is subject to change without notice. The University accepts no liability for any loss or damage howsoever arising from any use or misuse of or reliance on any information in this website.
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Personal Information Collection Statement. When you visit this website, we will have record of your Domain Name Server address and the pages you have visited. This information may be used by us for statistical purpose only.
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