Studies on sulfinatodehalogenation——XVIII. The reaction of perfluoroalkyl iodides with α-methylene cyclic ethers

Studies on sulfinatodehalogenation——XVIII. The reaction of perfluoroalkyl iodides with α-methylene cyclic ethers

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摘要 Perfluoroalkyl iodides reacted with various a-methylene oxacycloalkanes in the presence of sodium dithionite to give ring opening adducts. The reaction provided an efficient method for the syntheses of polyfunctional organofluorine compounds. Perfluoroalkyl iodides reacted with various a-methylene oxacycloalkanes in the presence of sodium dithionite to give ring opening adducts. The reaction provided an efficient method for the syntheses of polyfunctional organofluorine compounds.

作者 HUANG Wei-Yuan ZHANG Han-Zhong ZHUANG Jin-Lian

机构地区 Shanghai Instute of Organic Chemistry

出处《Chinese Journal of Chemistry》 SCIE CAS CSCD 1990年第6期555-560,共15页 中国化学(英文版)

关键词 methylene cyclic ethers The reaction of perfluoroalkyl iodides with XVIII

分类号 O6 [理学—化学]

引文网络
相关文献

1HU, Qiao-Sheng HU, Chang-Ming HUANG, Wei-YuanShanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China.Study on the sulfinatodehalogenation of BrCF_2CF_2R[J].Chinese Journal of Chemistry,1997,15(5):472-474.
2HUANG, Wei-Yuan,LU, Long,ZHANG, Yuan-Fa Shanghai Institute of Organic Chemistry, Academia Sinica, Shanghai 200032.Studies on sulfinatodehalogenation XVI.Sodium dithionite-initiated addition of perfluoroalkyl iodides to terminal alkynes[J].Chinese Journal of Chemistry,1990,8(4):350-354.
3HUANG,Wei-Yuan MA,Wu-Ping Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032.Studies on sulfinatodehalogenation ⅩⅩⅣ.Further study on sodium dithionite-initiated perfluoroalkylation of electron-rich aromatics[J].Chinese Journal of Chemistry,1992,10(2):180-185.
4HUANG Wei-Yuan,ZHANG Han-Zhong.Studies on sulfinatodehalogenation——ⅪⅩ.The reaction of perfluoroalkyl iodides and perfluoroalkane-sulfonyl bromides with conjugated dienes[J].Chinese Journal of Chemistry,1991,9(1):76-83.
5Fan Hong WU Bing Nan HUANG Shanghai Institute of Organic Chemistry,Academia Sinica,345 Lingling Lu,200032 Shanghai,.STUDIES ON SULFINATODEHALOGENATION:A NOVEL BROMODIFLUOROMETHYLATION METHOD[J].Chinese Chemical Letters,1993,4(8):683-686.
6HUANG Wei-Yuan,XIE Yuan-Lv,Long Shanghai.Studies on sulfinatodehalogenation——ⅩⅩ.Sodium dithionite-initiated addition of per-and polyfluoroalkyl iodides to cyclic enol ethers and chemical conversions of the products[J].Chinese Journal of Chemistry,1991,9(2):167-173.
7HUANG,Wei-Yuan LIU,Jin-Tao Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032.Synthesis and properties of p-per fluoroalkylcalix [4]arenes[J].Chinese Journal of Chemistry,1993,11(4):370-375.
8HUANG Wei-Yuan.Studies on sulfinatodehalogenation——ⅩⅪ.A new and convenient syntheses of 2-(F-alkyl)aldehydes,alcohols,acids and ketones[J].Chinese Journal of Chemistry,1991,9(2):174-180.
9HUANG, Bing-Nan,LIU,Jin-Tao Shanghai Institute of Organic Chemistry, Academia Sinica, Shanghai 200032.Studies on sulfinatodehalogenation XVII.The sulfinatodehalogenation of primary perfluoroalkyl iodides and bromides by Rongalite[J].Chinese Journal of Chemistry,1990,8(4):355-357.
10Qiao Sheng HU,Chang Ming HU and Wei Yuan HUANG(Laboratory of Organofluorine Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai, 200032).Studies on the Sulfinatodehalogenation Pt.30:Synthesis of Trifluorovinyl Compounds[J].Chinese Chemical Letters,1997,8(8):669-672.

Chinese Journal of Chemistry

1990年第6期

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Studies on sulfinatodehalogenation——XVIII. The reaction of perfluoroalkyl iodides with α-methylene cyclic ethers

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