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Formic azido

Tests conducted by the Eastman Kodak Company have shown that tert-butyl azidoformate [Formic acid, azido, -butyl ester], also known as iert-butoxy carbonyl azide and 1-BOC azide, is a thermally unstable, shock-sensitive compound (TNT equivalence 45%). [Pg.122]

Formic acid, azido-, tert-butyl ester (8) Carbonazidic acid, 1,1-dimethylethyl ester (9) (1070-19-5)... [Pg.187]

The following reaction illustrates conversion of a nitroxide radical-bearing alcohol by CDI and azide ion to a spin-labeled ester of azido formic acid, which is used for the labeling of amino acids, giving carbamates [137]... [Pg.70]

An analogous reaction was carried out with ter/-butyl alcohol to give the imidazolium carboxylate in 77% yield and the azido formic ester in 85% yield.[l37]... [Pg.70]

BUTYL AZIDOFORMATE (Formic add, azido-, /er/-butyl ester)... [Pg.78]

FORMATION AND PHOTOCHEMICAL WOLFF REARRANGEMENT OF CYCLIC a-DIAZO KETONES D-NORANDROST-5-EN-3 -0L-16-CARB0XYLIC ACIDS, 52, 53 FORMIC ACID, AZIDO—, tert-BUTYL ESTER, 50, 9 Formylation, with acetic formic anhydride, 50, 2 p-FORMYLBENZENESULFONAMIDE, ... [Pg.130]

The addition of nitrenes leads predominantly to the closed [6,6] bridged isomers. The corresponding [5,6] bridged isomer is - if at all - formed only in small amounts, probably via a direct addition to the [5,6] bond [394]. Nitrenes have been generated by thermolysis of azido-formic esters [172,395 00], photolysis of aroyl azides [401] or aryl azide [402], elimination of O-4-nitrophenylsulfonylalkylhydroxamic acid [403] or reaction of amines with Pb(OAc)4 [404]. [Pg.170]

Azidoformic esters such as 342 react with Cgg in a [2-tl] addition (Scheme 4.70), if the temperature is high enough to induce the loss of nitrogen prior to addition, otherwise a [3-1-2] addition can be observed (Section 4.3.2) [172, 395, 397]. Typical conditions include heating of the mixture in solvents such as tetrachloroethane [395, 397, 398], chloronaphfhalene [397] or toluene [396] at 110-160 °C. These conditions also afford multiple addition products [172]. To avoid potential hazard during purification of the azido formiates, they were also generated in situ in one pot by the reaction of chloro-formic ester with sodium azide [396]. [Pg.170]

SYNS t-BUTOXYCARBONYL AZIDE tert-BUTOXYCARBONYL AZIDE (DOT) ten-BUTYLOXY-CARBONYL AZIDE CARBONAZIDIC ACID, 1,1-DIMETHYLETHYL ESTER FORMIC ACID, AZIDO-, ten-BUTYL ESTER... [Pg.231]

Peptide synthesis, N-protection Acetic-formic anhydride. Adamantyl chloroformate. Benzylthiocarbonyl chloride. /-Butoxycarbonyl-N-hydroxysuccinimide ester. /-Butyl azido-formate. /-Butylcarbonic diethylphosphoric anhydride. /-Butyl fluoroformate. /-Butyl oxycarbonyl fluoride. /-Butyl pentachlorophenyl carbonate. /-Butyl 2,4,5-trichlorophenyl carbonate. Carbobenzoxy chloride. 3,5-Dimethoxybenzyl p-nitrophenyl carbonate. [2-(Diphenyl)isopropyljphenyl carbonate. /-Pentyl chloroformate. [Pg.243]

FORMIC ACID, AZIDO-, tert-BUTYL ESTER, 50, 9 Formylation, with acetic formic anhydride, SO, 2... [Pg.73]

Azido- from chloro-formic acid esters OCOCl OCON3... [Pg.120]


See other pages where Formic azido is mentioned: [Pg.249]    [Pg.825]    [Pg.33]    [Pg.1698]    [Pg.180]    [Pg.210]    [Pg.72]    [Pg.301]    [Pg.56]    [Pg.454]    [Pg.19]   


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