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Chen, Mao, Weng, Yue, Guo, Mian, Zhang, Hua, Lei, Aiwen (2008) Nickel-Catalyzed Reductive Cyclization of Unactivated 1,6-Enynes in the Presence of Organozinc Reagents. Angewandte Chemie International Edition, 47 (12). 2279-2282 doi:10.1002/anie.200704452

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Reference TypeJournal (article/letter/editorial)
TitleNickel-Catalyzed Reductive Cyclization of Unactivated 1,6-Enynes in the Presence of Organozinc Reagents
JournalAngewandte Chemie International Edition
AuthorsChen, MaoAuthor
Weng, YueAuthor
Guo, MianAuthor
Zhang, HuaAuthor
Lei, AiwenAuthor
Year2008 (March 7)Volume47
Issue12
PublisherWiley
DOIdoi:10.1002/anie.200704452Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID8584032Long-form Identifiermindat:1:5:8584032:0
GUID0
Full ReferenceChen, Mao, Weng, Yue, Guo, Mian, Zhang, Hua, Lei, Aiwen (2008) Nickel-Catalyzed Reductive Cyclization of Unactivated 1,6-Enynes in the Presence of Organozinc Reagents. Angewandte Chemie International Edition, 47 (12). 2279-2282 doi:10.1002/anie.200704452
Plain TextChen, Mao, Weng, Yue, Guo, Mian, Zhang, Hua, Lei, Aiwen (2008) Nickel-Catalyzed Reductive Cyclization of Unactivated 1,6-Enynes in the Presence of Organozinc Reagents. Angewandte Chemie International Edition, 47 (12). 2279-2282 doi:10.1002/anie.200704452
In(2008, March) Angewandte Chemie International Edition Vol. 47 (12) Wiley

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Chen, Mao, Weng, Yue, Guo, Mian, Zhang, Hua, Lei, Aiwen (2008) Nickel-Catalyzed Reductive Cyclization of Unactivated 1,6-Enynes in the Presence of Organozinc Reagents. Angewandte Chemie, 120 (12). 2311-2314 doi:10.1002/ange.200704452
Takachi, Manabu, Kita, Yusuke, Tobisu, Mamoru, Fukumoto, Yoshiya, Chatani, Naoto (2010) Nickel-Catalyzed Cyclization of Difluoro-Substituted 1,6-Enynes with Organozinc Reagents through the Stereoselective Activation of CF Bonds: Synthesis of Bicyclo[3.2.0]heptene Derivatives. Angewandte Chemie International Edition, 49 (46). 8717-8720 doi:10.1002/anie.201004543
Wang, Kuai, Chen, Jiachang, Liu, Wenfeng, Kong, Wangqing (2022) Nickel‐Catalyzed Defluorinative Asymmetric Cyclization of Fluoroalkyl‐Substituted 1,6‐Enynes for the Synthesis of Seletracetam. Angewandte Chemie International Edition, 61 (46) doi:10.1002/anie.202212664
Hu, Shengwei, Wang, Xiaoqin, Wu, Tianbao, Ding, Zhengtian, Wang, Minyan, Kong, Wangqing (2025) Ni‐Catalyzed Enantioselective Reductive Cyclization/Amidation and Amination of 1,6‐Enynes and 1,7‐Enynes. Angewandte Chemie International Edition, 64 (1). doi:10.1002/anie.202413892
Liu, Wei, Cao, Hao, Lei, Aiwen (2010) Iron-Catalyzed Direct Arylation of Unactivated Arenes with Aryl Halides. Angewandte Chemie International Edition, 49 (11). 2004-2008 doi:10.1002/anie.200906870
You, Yang'en, Ge, Shaozhong (2021) Asymmetric Cobalt‐Catalyzed Regioselective Hydrosilylation/Cyclization of 1,6‐Enynes. Angewandte Chemie International Edition, 60 (21) 12046-12052 doi:10.1002/anie.202100775
Chen, Jiahua, Hayashi, Tamio (2020) Asymmetric Synthesis of Alkylzincs by Rhodium‐Catalyzed Enantioselective Arylative Cyclization of 1,6‐Enynes with Arylzincs. Angewandte Chemie International Edition, 59 (42) 18510-18514 doi:10.1002/anie.202008770
Yin, Guoyin, Liu, Guosheng (2008) Palladium‐Catalyzed Oxidative Cyclization of Enynes with Hydrogen Peroxide as the Oxidant. Angewandte Chemie International Edition, 47 (29). 5442-5445 doi:10.1002/anie.200801438
Serrano, Eloisa, Martin, Ruben (2016) Nickel-Catalyzed Reductive Amidation of Unactivated Alkyl Bromides. Angewandte Chemie International Edition, 55 (37). 11207-11211 doi:10.1002/anie.201605162
Jin, Youxiang, Wang, Chuan (2019) Nickel‐Catalyzed Asymmetric Reductive Arylalkylation of Unactivated Alkenes. Angewandte Chemie International Edition, 58 (20). 6722-6726 doi:10.1002/anie.201901067
Bae, Hyo J., Baskar, Baburaj, An, Sang E., Cheong, Jae Y., Thangadurai, Daniel T., Hwang, In-Chul, Rhee, Young H. (2008) Gold(I)-Catalyzed Cycloisomerization of 3-Methoxy-1,6-enynes Featuring Tandem Cyclization and [3,3]-Sigmatropic Rearrangement. Angewandte Chemie International Edition, 47 (12). 2263-2266 doi:10.1002/anie.200705117
 
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