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Solid-phase multi-step syntheses

Carbo-2-(p-diphenyl)isopropoxy derivatives. N-2-(p-Diphenyl)isopropyloxycarbo-nylleucine stirred 1.5 hrs. at room temp, with acetic acid-formic acid-water (7 1 2) leucine. Y 94%. - Of a number of N-aralkoxycarbonyl protective groups tested 2-(p-diphenyl)isopropyloxycarbonyl was the most suitable for peptide syntheses (Helv. 51y 614). Selective and preferential removal in the presence of other acid-labile protective groups, especially those derived from rerr-butanol, also application in solid-phase multi-step syntheses, s. P. Sieber and B. Iselin, Helv. 51 y 622, 614 (1968). [Pg.293]

Merrifield syntheses (s. a. Solid-phase multi-step syntheses)... [Pg.266]

Hydrogen bromide acetic acid Solid phase multi-step syntheses Peptides... [Pg.19]

See other pages where Solid-phase multi-step syntheses is mentioned: [Pg.249]    [Pg.275]    [Pg.276]    [Pg.306]    [Pg.296]    [Pg.338]    [Pg.299]    [Pg.266]    [Pg.270]    [Pg.271]    [Pg.270]    [Pg.272]    [Pg.280]    [Pg.270]    [Pg.279]    [Pg.288]    [Pg.290]   


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MULTI PHASE

Multi-step synthesis

Solid-phase multi-step

Solid-phase synthesi

Synthesis step

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