α-Nitrohydrazones: versatile intermediates for phosphonate derivatives formation from primary nitro compounds
Primary nitro compounds can be easily converted into hydrazonophosphonate derivatives through coupling with aryldiazonium salts followed by an Arbuzov-type reaction with phosphite. Graphic
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Published in | Tetrahedron letters Vol. 43; no. 11; pp. 2037 - 2038 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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11.03.2002
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Abstract | Primary nitro compounds can be easily converted into hydrazonophosphonate derivatives through coupling with aryldiazonium salts followed by an Arbuzov-type reaction with phosphite.
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AbstractList | Primary nitro compounds can be easily converted into hydrazonophosphonate derivatives through coupling with aryldiazonium salts followed by an Arbuzov-type reaction with phosphite. (C) 2002 Elsevier Science Ltd. All rights reserved. Primary nitro compounds can be easily converted into hydrazonophosphonate derivatives through coupling with aryldiazonium salts followed by an Arbuzov-type reaction with phosphite. Graphic |
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Author | El Kaı̈m, L Grimaud, L Jana, N.K Tirla, C |
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ALPHA-AMINOBENZYLPHOSPHONIC ACID publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: KOSOLAPOFF, GM – volume: 75 start-page: 604 year: 1963 ident: WOS:A19634269A00005 article-title: 1.3-DIPOLARE CYCLOADDITIONEN - RUCKSCHAU UND AUSBLICK publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION contributor: fullname: HUISGEN, R – start-page: 909 year: 1979 ident: WOS:A1979HV49900018 article-title: SYNTHESIS OF 2-SUBSTITUTED 4H-[1,2,4]TRIAZOLO[5,1-C][1,4]BENZOXAZINES publication-title: SYNTHESIS-STUTTGART contributor: fullname: BIZZOZERO, N – start-page: 1028 year: 1980 ident: WOS:A1980KV18600021 article-title: SYNTHESIS OF O,O-DIALKYL 1-AMINOALKANEPHOSPHONATES publication-title: SYNTHESIS-STUTTGART contributor: fullname: KUDZIN, ZH – volume: 31 start-page: 2632 year: 1898 ident: WOS:000174601000027.1 publication-title: CHEM BER contributor: fullname: BAMBERGER E – volume: 10 start-page: 142 year: 1971 ident: WOS:000174601000027.12 publication-title: METHODEN ORGANISCHEM contributor: fullname: PADEKEN HG – volume: 19 start-page: 905 year: 1982 ident: WOS:A1982PG08600038 article-title: BASE-PROMOTED CYCLIZATION OF 1-NITROHYDRAZONES BEARING A THIOETHER FUNCTION publication-title: JOURNAL OF HETEROCYCLIC CHEMISTRY contributor: fullname: BRUCHE, L – volume: 116 start-page: 3039 year: 1983 ident: WOS:A1983RG88800004 article-title: 1,3-DIPOLAR CYCLO-ADDITIONS .88. 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Heterocyclic Chem. doi: 10.1002/jhet.5570170606 contributor: fullname: Hassaneen – start-page: 689 year: 1987 ident: 10.1016/S0040-4039(02)00208-3_BIB9 publication-title: Synthesis doi: 10.1055/s-1987-28046 contributor: fullname: Rösch – volume: 116 start-page: 3039 year: 1983 ident: 10.1016/S0040-4039(02)00208-3_BIB4 publication-title: Chem. Ber. doi: 10.1002/cber.19831160905 contributor: fullname: Fliege – volume: 31 start-page: 2632 year: 1898 ident: 10.1016/S0040-4039(02)00208-3_BIB12 publication-title: Chem. Ber. contributor: fullname: Bamberger – ident: 10.1016/S0040-4039(02)00208-3_BIB2 – volume: 12 start-page: 1028 year: 1980 ident: 10.1016/S0040-4039(02)00208-3_BIB11 publication-title: Synthesis doi: 10.1055/s-1980-29311 contributor: fullname: Kudzin – start-page: 909 year: 1979 ident: 10.1016/S0040-4039(02)00208-3_BIB6 publication-title: Synthesis doi: 10.1055/s-1979-28872 contributor: fullname: Bizzozero – ident: 10.1016/S0040-4039(02)00208-3_BIB1 – start-page: 814 year: 1974 ident: 10.1016/S0040-4039(02)00208-3_BIB5 publication-title: Synthesis doi: 10.1055/s-1974-23442 contributor: fullname: Garanti – volume: 70 start-page: 1283 year: 1948 ident: 10.1016/S0040-4039(02)00208-3_BIB10 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja01183a513 contributor: fullname: Kosolapoff |
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Snippet | Primary nitro compounds can be easily converted into hydrazonophosphonate derivatives through coupling with aryldiazonium salts followed by an Arbuzov-type... |
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Title | α-Nitrohydrazones: versatile intermediates for phosphonate derivatives formation from primary nitro compounds |
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