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Posted: 18.03.05 00:31. Post subject: Re: Производные азодикарбоновой кислоты
В ССD про азодикарбонимид немного:
Entry Name: 3H-1,2,4-Triazole-3,5(4H)-dione, 9CI
Synonym(s): 1,2,4-Triazoline-3,5-dione
Chapman Hall Number: BMZ06-P
CAS Registry Number: 4019-43-6
Molecular Formula: C2HN3O2
Molecular Weight: M 99.049.
Use/Importance: Synthon, reactive dienophile.
Physical Description: Red.
Other Data: .lambda.max 504 sh, 520, 540 and 563 nm.
Есть N-алкил-производные и N-п-нитрофенил и все.
Но можно порыться в литературе, данной в конце записи:
References:
Aldrich Library of 13C and 1H FT NMR Spectra,1, 1323C (nmr)
Cookson, RC et al.,J.C.S.(C),1967, 1905 (synth, deriv)
Fieser and Fieser’s Reagents for Organic Synthesis,Wiley, 1969, 2, 282; ,1979, 7, 287; ,1992, 16, 223 (use)
Org. Synth.,1971, 51, 121 (deriv, synth, ir, uv)
Moore, JA et al.,J.O.C.,1974, 39, 3799 (deriv, synth)
Womhoff, H et al.,Org. Prep. Proced. Int.,1975, 7, 251 (deriv, synth)
Adam, W et al.,Angew. Chem., Int. Ed.,1980, 19, 762 (rev, deriv)
Womhoff, H et al.,Angew. Chem., Int. Ed.,1981, 20, 797 (synth, bibl)
Cheng, C-C et al.,J.O.C.,1984, 49, 2910, 2917 (deriv, use)
Moriarty, RM et al.,Synth. Commun.,1987, 17, 409 (synth)
Young, DC et al.,J. Chromatogr.,1990, 522, 295 (use)
Myers, AG et al.,J.A.C.S.,1990, 112, 9641
Nelsen, SF et al.,J.O.C.,1991, 56, 613 (synth)
Про азодикарбонгидразид тоже не много:
Entry Name: 1,2-Dihydro-1,2,4,5-tetrazine-3,6-dione, 9CI
Synonym(s): 1,2,4,5-Tetrazine-3,6-diol. 6-Hydroxy-1,2,4,5-tetrazin-3(2H)-one. 3,6-Dihydroxy-1,2,4,5-tetrazine
Chapman Hall Number: GWZ99-O
CAS Registry Number: 81930-28-1
Molecular Formula: C2H2N4O2
Molecular Weight: M 114.063.
Physical Description: Orange-brown cryst. (Me2CO/petrol).
Melting Point: Mp 168 deg (explodes).
Derivative: Di-Me ether
Synonym(s): 3,6-Dimethoxy-1,2,4,5-tetrazine
Chapman Hall Number: GXB00-V
CAS Registry Number: 81930-31-6
Molecular Formula: C4H6N4O2
Molecular Weight: M 142.117.
Physical Description: Red-violet needles (C6H6).
Melting Point: Mp 62-63 deg.
References:
Neugebauer, FA et al.,Annalen,1982, 387 (synth, ir, uv, pmr)
Krieger, C et al.,Acta Cryst. C,1987, 43, 1412 (cryst struct, deriv)
Надеюсь, хоть как-то помог ;-).
А что насчет деталей?
Вот, книги некоторые ищу (задумчиво так...)
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