255. Visible-Light-Driven Photocatalytic Kharasch Reaction of Phenol/Arylamine-Linked 1,6-Enynes with
Perhalogenated Methane
Xiaoshuang Ji, Rong Fu, Shuliang Wang*, Wenjuan Hao, Bo Jiang*
Chin. J. Org. Chem. 2022, 42, 4282-4291; DOI: 10.6023/cjoc202211011 [Link]
254. Azoarene activation for Schmidt-type reaction and mechanistic insights
Fan-Tao Meng, Ya-Nan Wang, Xiao-Yan Qin, Shi-Jun Li, Jing Li, Wen-Juan Hao,* Shu-Jiang Tu, Yu Lan,*
Bo Jiang*
Nat. Commun. 2022, 13, 7393; DOI:10.1038/s41467-022-35141-4 [Link]
253. A Solvent-Regulated Dediazotized Oxygenation of α-Aryl α-Diazoesters and 2,3-Dichloro-5,6-dicyano-
1,4-benzoquinone (DDQ)
Runhong Jia,* Shuai Liu, Shichao Wang, Wenjuan Hao, Bo Jiang*
Chin. J. Org. Chem. 2022, 42, 2814-2822 [Link]
252. Regio- and Enantioselective Synthesis of Dihydropyrido[1,2-a]indoles via Catalytic Asymmetric
Annulative Allylic Alkylation
Xue Wang, Hui-Lin Mao, Yu-Heng Yang, Hong Jiang, Ling-Qi Chen, Shu-Jiang Tu,* Wen-Juan Hao,* Bo Jiang*
J. Org. Chem. 2022, 87, 15644-15652; DOI:10.1021/acs.joc.2c01873 [Link]
251. Electrochemical selective annulative amino-ketalization and amino-oxygenation of 1,6-enynes
Xiao-Shuang Ji, Hang-Dong Zuo, Yi-Ting Shen, Wen-Juan Hao,* Shu-Jiang Tu,* Bo Jiang*
Chem. Commun. 2022, 58, 10420-10423; DOI: 10.1039/D2CC03922B [Link]
250. Photocatalytic Chemodivergent Synthesis of α-gem-Dihalovinyl Ketones and Chromen-2-ones from
Monoalkynes
Zi-Yang Xu, Yin-Ping Liu, Xin Liu, Rong Fu, Wen-Juan Hao,* Shu-Jiang Tu,* Bo Jiang*
Adv. Synth. Catal. 2022, 364, 2666-2672; DOI: 10.1002/adsc.202200422 [Link]
249. Catalytic Enantioselective Construction of 6-4 Ring-Junction All-Carbon Stereocenters and Mechanistic
Insights
Jia-Yin Wang, Chen-Long Li, Ting Xu, Meng-Fan Li, Wen-Juan Hao, Shu-Jiang Tu, Jianyi Wang,* Guigen Li,
Zhi-Xiang Yu,* Bo Jiang*
Chin. J. Chem. 2022, 40, 1767-1776; DOI: 10.1002/cjoc.202200211 (Breaking Report) [Link]
248. Nitrative bicyclization of 1,7-diynes for accessing skeletally diverse tricyclic pyrroles
Lu Wang, Yin Zhang, An-Qi Miao, Tian-Shu Zhang,* Xiang Wang, Wen-Juan Hao,* Shu-Jiang Tu, Bo Jiang*
Chem. Commun. 2022, 58, 4376-4379; DOI: 10.1039/D2CC00206J [Link]
247. Engaging Yne-Allenes in Cycloaddition Reactions: Recent Developments
Jia-Yin Wang, Wen-Juan Hao,* Shu-Jiang Tu,* Bo Jiang*
Chin. J. Chem. 2022, 40, 1224-1242; DOI: 10.1002/cjoc.202100856 (Invited Review) [Link]
246. Diastereoselective Generation of C2-Azlactonized 2H-Chromenes via Brønsted acid-Catalyzed
Oxo-Cyclization of Propargyl Alcohols
Meng-Ying Hao, Min-Hua Huang, Xin-Yu Gu, Tian-Shu Zhang, Xiao-Tong Zhu,* Wen-Juan Hao,* Bo Jiang*
J. Org. Chem. 2022, 87, 1518-1525; DOI: 10.1021/acs.joc.1c02299 [Link]
245. Gold Self-Relay Catalysis Enabling [3,3]-Sigmatropic Rearrangement/Nazarov Cyclization and Allylic
Alkylation Cascade for Constructing All-Carbon Quaternary Stereocenters
Fan-Tao Meng, Xiao-Yan Qin, Jing Li, Tian-Shu Zhang,* Shu-Jiang Tu, Bo Jiang,* Wen-Juan Hao*
Chin. J. Chem. 2022, 40, 687-692; DOI: 10.1002/cjoc.202100734 [Link]
244. Gold self-relay catalysis for accessing functionalized cyclopentenones bearing an all-carbon quaternary
stereocenter
Fan-Tao Meng, Jing-Long Chen, Xiao-Yan Qin, Tian-Shu Zhang,* Shu-Jiang Tu, Bo Jiang,* Wen-Juan Hao*
Org. Chem. Front. 2022, 9, 140-146; DOI: 10.1039/D1QO01313K [Link]
243. Kharasch-type photocyclization of 1,7-diynes for the stereospecific synthesis of tetrahydronaphthalen-1-ols
Jia-Lin Zheng, Dan Wu, Na Lin, Yin-Ping Liu, Lu Wang, Xiao-Tong Zhu,* Wen-Juan Hao, Shu-Liang Wang,*
Bo Jiang*
Tetrahedron Lett. 2021, 85, 153485; DOI: 10.1016/j.tetlet.2021.153485 [Link]
242. Pd-Catalyzed Asymmetric Addition of Arylboronic Acids to Pyrazolinone Ketimines
An-Qi Miao, Meng Zhou, Jing-Long Chen, Shi-Chao Wang, Wen-Juan Hao,* Shu-Jiang Tu,* Bo Jiang*
Adv. Synth. Catal. 2021, 363, 5162-5166; DOI: 10.1002/adsc.202101137 [Link]
241. Cyclic oxime esters as deconstructive bifunctional reagents for cyanoalkylesterification of 1,6-enynes
Shi-Chao Wang, Yi-Ting Shen, Tian-Shu Zhang,* Wen-Juan Hao,* Shu-Jiang Tu, Bo Jiang*
J. Org. Chem. 2021, 86, 15488-15497; DOI: 10.1021/acs.joc.1c01972 [Link]
240. Photocatalytic biheterocyclization of 1,7-diynes for accessing skeletally diverse tricyclic 2-pyranones
Lu Wang, Ting Xu, Qian Rao, Tian-Shu Zhang,* Wen-Juan Hao,* Shu-Jiang Tu, Bo Jiang*
Org. Lett. 2021, 23, 7845-7850; DOI:10.1021/acs.orglett.1c02865 [Link]
239. Photocatalytic three-component annulation enabling stereoselective generation of (Z)-thiochromene
1,1-dioxides
Ke-Xian Song, Xiao-Yan Qin, Zi-Xuan Ma, Fang-Zhou Geng, Wen-Juan Hao,* Shu-Jiang Tu, Bo Jiang*
Org. Chem. Front. 2021, 8, 5681-5686; DOI: 10.1039/D1QO00994J [Link]
238. Visible-Light-Driven Photocatalytic Kharasch-Type Addition of 1,6-Enynes
Fang-Zhou Geng, Shi-Chao Wang, Ke-Xian Song, Wen-Juan Hao,* Bo Jiang*
Chin. J. Org. Chem. 2021, 41, 4815-4824; DOI: 10.6023/cjoc202106014 [Link]
可见光催化的1,6-烯炔参与的Kharasch加成反应
耿芳洲, 王世超, 宋克贤, 郝文娟,*姜波*
有机化学 2021, 41, 4815-4824; DOI: 10.6023/cjoc202106014 (Invited for 绿色化学专辑)
237. Copper/silver co-mediated three-component bicyclization for accessing indeno[1,2-c]azepine-3,6-diones
Shi-Chao Wang, Peng-Yu Liu, Yi-Xin Chen, Zheng-Jia Shen, Wen-Juan Hao,* Shu-Jiang Tu,* Bo Jiang*
Chem. Commun. 2021, 57, 7966-7969; DOI:10.1039/D1CC02973H [Link]
236. Gold-Catalyzed Skeletal Rearrangement of Alkenes: Regioselective Synthesis of Skeletally Diverse Tricyclic
Heterocycles and Mechanistic Investigations
Xiao-Yan Qin, Fan-Tao Meng, Mian Wang, Shu-Jiang Tu,* Wen-Juan Hao, Jianyi Wang,* Bo Jiang*
ACS Catal. 2021, 11, 6951–6959; DOI: 10.1021/acscatal.1c00753 [Link]
235. Enantio- and Regioselective CuH-Catalyzed Conjugate Reduction of Yne-Allenones
Jia-Yin Wang, Guigen Li,* Wen-Juan Hao, Bo Jiang*
Org. Lett. 2021, 23, 3828-3833; DOI:10.1021/acs.orglett.1c00892 [Link]
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234. Copper-Catalyzed Asymmetric Deconstructive Alkynylation of Cyclic Oximes
Hang-Dong Zuo, Shan-Shan Zhu, Wen-Juan Hao,* Shi-Chao Wang, Shu-Jiang Tu,* Bo Jiang*
ACS Catal. 2021, 11, 6010-6019; DOI: 10.1021/acscatal.1c00842 [Link]
233. Engaging yne-allenones in tunable catalytic silane-mediated conjugate transfer reductions
Xiao-Yan Qin, Jia-Yin Wang, Fang-Zhou Geng, Wen-Juan Hao,* Shu-Jiang Tu,* Bo Jiang*
Chem. Commun. 2021, 57, 5394-5397; DOI: 10.1039/D1CC01422F [Link]
232. Diastereoselective Synthesis of 1,2-Dihydrobenzofuro[3,2-b]pyridines via a Carbon-Carbon
Double Bond Cleavage–Rearrangement Cascade
Chi-Fan Zhu, Ling-Qi Chen, Wen-Juan Hao,* Chen-Chang Cui, Shu-Jiang Tu,* Bo Jiang*
Org. Lett. 2021, 23, 2654-2658; DOI: 10.1021/acs.orglett.1c00564 [Link]
231. Synthesis of Fused Pyridines via Microwave-Assisted [3 + 3] Cyclization
Yanan Wu*, Jianyu Du, Wenjuan Hao, Bo Jiang*
Chin. J. Org. Chem. 2021, 41, 1563-1571; DOI: 10.6023/cjoc202102018 [Link]
利用微波辅助[3+3]环化反应合成稠合吡啶衍生物
吴亚男*, 杜建宇, 郝文娟, 姜波*
有机化学 2021, 41, 1563-1571; DOI: 10.6023/cjoc202102018
230. Study on tert-Butyl Radical-Initiated 1,2-Alkynyl Migration
Ping Zhang, Tian-Shu Zhang, Pei-Jun Cai,* Bo Jiang, Shu-Jiang Tu*
Chin. J. Org. Chem. 2021, DOI:10.6023/cjoc202101042 [Link]
叔丁基自由基引发的1,2-炔基迁移反应研究
张萍, 张天舒, 蔡佩君*, 姜波, 屠树江*
有机化学 2021, DOI:10.6023/cjoc202101042
229. Sc(OTf)3-Catalyzed Dearomatization of Indoles for the Synthesis of 3,3’-Bisindoles
Rong Wang, Lichen Xu, Yi Lu, Bo Jiang*, Wenjuan Hao*
Chin. J. Org. Chem. 2021, 41, 1582-1590; DOI:10.6023/cjoc202101003 [Link]
利用三氟甲基磺酸钪催化的吲哚去芳构化反应合成3,3’-双吲哚衍生物
王榕,徐立晨,卢逸,姜波*,郝文娟*
有机化学 2021, 41, 1582-1590; DOI:10.6023/cjoc202101003
228. Regio- and Stereoselective Synthesis of Rotationally Hindered C12-Naphthylated Tribenzo[a,c,j]xanthenes
through Catalytic Tricyclization of Yne-Allenones
Shan-Shan Zhu, Heng Li, Rong Fu, Wen-Juan Hao*, Shu-Liang Wang, Shu-Jiang Tu, Bo Jiang*
Adv. Synth. Catal. 2021, 363, 2199-2204; DOI:10.1002/adsc.202100061 [Link]
227. Photoinduced arene-alkyne [3 + 2] cycloaddition cascade of 1-alkynylnaphthalen-2-ols for tunable
synthesis of skeletally diverse bridged hexacycles
Chi-Fan Zhu, Jie Zhang, Yi-Long Zhu*, Wen-Juan Hao, Shu-Jiang Tu, De-Cai Wang*, Bo Jiang*
Org. Chem. Front. 2021, 8, 1952-1958; DOI: 10.1039/D1QO00124H [Link]
226. Synthesis of Fully Substituted Oxazoles via an NFSI/KF-Mediated Double Bond
Cleavage-Rearrangement Cascade
Dan Wu, Yi Lu, Wen-Juan Hao*, Shu-Jiang Tu, Bo Jiang*
Asian J. Org. Chem. 2021, 10, 602-605; DOI: 10.1002/ajoc.202000627 [Link]
225. Tunable Electrocatalytic Annulations of o-Arylalkynylanilines: Green and Switchable
Syntheses of Skeletally Diverse Indoles
Jie Zhang, Shao-Qing Shi, Wen-Juan Hao*, Guo-Yun Dong, Shu-Jiang Tu*, Bo Jiang*
J. Org. Chem. 2021, 86, 15886–15896; DOI: 10.1021/acs.joc.0c02898 [Link]
224. Cu-Catalyzed radical-triggered spirotricyclization of enediynes and enyne-nitriles for the
synthesis of pentacyclic spiroindenes
Hang-Dong Zuo, Xiao-Shuang Ji, Cheng Guo*, Shu-Jiang Tu, Wen-Juan Hao*, Bo Jiang*
Org. Chem. Front. 2021, 8, 1496-1502; DOI:10.1039/D0QO01640C [Link]
223. Engaging 1,7-diynes in a photocatalytic Kharasch-type addition/1,5-(SN'')-substitution
cascade toward β-gem-dihalovinyl carbonyls
Dan Wu, Wen-Juan Hao*, Qian Rao, Yi Lu, Shu-Jiang Tu*, Bo Jiang*
Chem. Commun. 2021, 57, 1911-1914; DOI: 10.1039/D0CC07880H [Link]
222. Generation of stereodefined (Z)-3,4-dihydronaphthalen-1(2H)-ones via
copper-catalyzed annulation-cyanotrifluoromethylation of 1,7-enynes
Wen-Zhe Ji, Hao-Nan Shi, Wen-Juan Hao, Ping Wei*, Shu-Jiang Tu, Bo Jiang*
Tetrahedron Lett. 2021, 64, 152722; DOI: 10.1016/j.tetlet.2020.152722 [Link]
221. Photocatalytic Annulation-Carbohalogenation of 1,7-Enynes for Atom-Economic
Synthesis of Functionalized 3,4-dihydronaphthalen-1(2H)-ones
Wen-Zhe Ji, Hao-Nan Shi, Ping Wei*, Wen-Juan Hao, Shu-Jiang Tu, Bo Jiang*
Adv. Synth. Catal. 2021, 363, 838-845; DOI: 10.1002/adsc.202001125 [Link]
220. Synthesis of C3-alkylated benzofurans via palladium-catalyzed regiocontrolled
hydro-furanization of unactivated alkenes
Chi-Fan Zhu, Cong-Hui Gao, Wen-Juan Hao, Yi-Long Zhu*, Shu-Jiang Tu, De-Cai Wang*, Bo Jiang*
Org. Chem. Front. 2021, 8, 127-132; DOI: 10.1039/D0QO01247E [Link]
219. Dual Palladium/Scandium Catalysis toward Rotationally Hindered C3-Naphthylated Indoles from β-Alkynyl
Ketones and o-Alkynyl Anilines
Dan Wang, Shi-Chao Wang, Wen-Juan Hao, Shu-Jiang Tu,* Bo Jiang*
Chin. J. Chem. 2021, 39, 106-114; DOI: 10.1002/cjoc.202000304 [Link]
