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Azides protecting group

Organic Azides Protective Group, Masked Amines... [Pg.46]

Treatment of 8-azidomethylperhydropyrido[l,2-c]pyrimidin-l-one 157 with methyl triflate and catalytic hydrogenation of the azide group led to the formation of tricyclic guanidine derivative 158 (01JA8851). Hydroxy group of 149 was protected with methoxymethyl chloride, and the p-methoxybenzyl protecting group (PMB) was eliminated by treatment with DDQ. [Pg.254]

See other pages where Azides protecting group is mentioned: [Pg.390] [Pg.2948] [Pg.390] [Pg.2948] [Pg.61] [Pg.174] [Pg.254] [Pg.446] [Pg.15] [Pg.577] [Pg.534] [Pg.248] [Pg.64] [Pg.226] [Pg.51] [Pg.65] [Pg.79] [Pg.248] [Pg.249] [Pg.342] [Pg.343] [Pg.660] [Pg.26] [Pg.101] [Pg.384] [Pg.281] [Pg.166] [Pg.272] [Pg.58] [Pg.114] [Pg.437] [Pg.199] [Pg.1522] [Pg.118] [Pg.111] [Pg.112] [Pg.71] [Pg.268] [Pg.663] [Pg.674] [Pg.9] [Pg.209] [Pg.241] [Pg.269]

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Azides as Protecting Groups during Aminoglycoside Synthesis

Azides groups