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L- aziridine

Primary allyUc amines.l Aziridines can be converted into allyl carbamates by reaction with ethyl chloroformate to form N-ethoxycarbonylaziridines followed by thermolysis in benzene at 200-250°. Rearrangement of trisubstituted ethoxycarbonylaziridines is regiospecific. [Pg.223]

TRIS(ALLYLOXY)TRLAZINE see THN500 TRIS(AMINOETHYL)AMINE see NEI800 TRIS( -AMINOETHYL)AMINE see NEI800 TRIS(l-AZIRIDINE)PHOSPHINE OXIDE see TND250... [Pg.1925]

IH-Aziridines. In the presence of BF3 etherate, this reagent adds to double bonds substituted with three cyano or carboalkoxy groups to give an adduct that is converted into a l//-aziridine by treatment with triethylamine. [Pg.132]

S),25-epiminolanosterol (116) was a potent noncompetitive inhibitor (Kj = 3.0 nM) of the 5-adenosyl-L-methi(Miine-C-24 Me transferase from sunflower embryos [127]. Cholesteryl ester of l-aziridine acetic acid (117) showed excellent inhibition of a dimethyl-benzanthrene induced and transplantable mammary adenocarcinoma [128]. [Pg.994]

CgHsNHNH, (CgH,)2N-N(CgHg)2 N-A minopheny l-aziridine Girard reagents Tosylhydrazine Benzalazine HN.NH... [Pg.671]

The photoirradiation of l-(2-naphthc l)aziridine in halogenated hydrocarbon solvents gave a canplex mixture of products amongst vhich... [Pg.42]


See other pages where L- aziridine is mentioned: [Pg.548]    [Pg.2054]    [Pg.2058]    [Pg.279]    [Pg.2054]    [Pg.2054]    [Pg.54]    [Pg.54]    [Pg.191]    [Pg.1564]    [Pg.7]    [Pg.458]    [Pg.2054]    [Pg.2058]    [Pg.2169]    [Pg.2224]    [Pg.2250]    [Pg.2251]    [Pg.2251]    [Pg.2252]    [Pg.2252]    [Pg.2306]    [Pg.273]    [Pg.1148]    [Pg.1148]    [Pg.1148]    [Pg.1175]    [Pg.293]   
See also in sourсe #XX -- [ Pg.6 ]




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Aziridine, l- synthesis

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