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Synthesis 2003(2): 0195-0197
DOI: 10.1055/s-2003-36814
DOI: 10.1055/s-2003-36814
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York
The Reaction of Bu3P-CS2 Adduct with Azo Compounds and Aromatic Aldehydes
Further Information
Received
9 May 2002
Publication Date:
22 January 2003 (online)
Publication History
Publication Date:
22 January 2003 (online)
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Abstract
Bu3P-CS2 adduct, generated from tributylphosphine and carbon disulfide, reacted with dialkyl azodicarboxylates and aromatic aldehydes in one-pot to give 1,3,4-thiadiazolidine-2-thiones.
Key words
tributylphosphine - carbon disulfide - dialkyl azodicarboxylates - thiadiazolidine-2-thiones
- 1
Klepel M,Held P, andTschampel G. inventors; German Patent (East) 100136. ; Chem. Abstr. 1974, 80, 104876 - 2
Uchida A.Iida T.Sato Y.Boger P. Z. Naturforsch., C: Biosci. 1997, 52: 345 ; Chem. Abstr. 1997, 127, 161761 - 3
Iida T.Uchida A.Uraguchi R.Sato Y.Boger P.Wakabayashi K. Nippon Noyaku Gakkaishi 1997, 22: 303 ; Chem. Abstr. 1998, 128, 58544 - 4
Zhang YY.Ding Y.Zhang YB.Chen YQ. Chin. Chem. Lett. 1996, 7: 309 ; Chem. Abstr. 1996, 125, 34027 - 5
Zhang YY.Ding Y.Zhang YB.Chen YQ. Huaxue Xuebao 1997, 55: 411 ; Chem. Abstr. 1997, 126, 317555 - 6
Ding Y.Zhang YY.Zhang J.Chen YQ. Bioorg. Med. Chem. Lett. 1997, 7: 1607 - 7
Heugebaert FC, andWillems JF. inventors; US Patent 3474108. ; Chem. Abstr. 1969, 71, 124439 - 8
Heugebaert FC.Willems JF. Tetrahedron 1966, 22: 913 - 9
Mayer KH.Lauerer D. Liebigs Ann. Chem. 1970, 731: 142 - 10
Anthom U.Larsen C.Nielsen PH. Acta Chem. Scand. 1970, 24: 179 - 11
Ali MA.Livingstone SE.Phillips DJ. Inorg. Chim. Acta 1973, 7: 553 - 12 inventors; ;
French Patent 2306205. ICI Australia Ltd.
; Chem. Abstr. 1977, 87, 39260
- 13
Serban A,Warner RB, andAlcock KT. inventors; US Patent 4064262. ; Chem. Abstr. 1978, 88, 120967 - 14
Motoyoshiya J.Nishijima M.Yamamoto I. J. Chem. Soc., Perkin Trans. 1 1980, 574 - 15
Scovill JP.Silverton JV. J. Org. Chem. 1980, 45: 4372 - 16
Karl IL.Karlr J.Moriarty RM. Tetrahedron Lett. 1964, 47: 3579 - 17
Grashey R.Huisgen R.Sun KK. J. Org. Chem. 1965, 30: 74 - 18
Chen XD.Liu YX.Xue M.Cao RZ.Liu LZ. Phosphorus, Sulfur Silicon Relat. Elem. 1999, 152: 185 - 19
Xu CF.Liu YX.Cao RZ.Liu LZ. Synth. Commun. 2002, 32: 535 - 21
Guthrie RD.Jenkins ID. Aust. J. Chem. 1982, 35: 767 - 22
Huang S. Handbook of Preparation of Organic Syntheses Reagents Sichuan University Publishing House; China: 1988. p.186-187
References
Xu, C. F.; Liu Y. X.; Cao, R. Z.; Liu, L. Z. Heteroatom, in press.