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Pyrrolidine-2-carboxylic acid esters, 3-hydroxy- from

In peptide syntheses, where partial racemization of the chiral a-carbon centers is a serious problem, the application of 1-hydroxy-1 H-benzotriazole ( HBT") and DCC has been very successful in increasing yields and decreasing racemization (W. Kdnig, 1970 G.C. Windridge, 1971 H.R. Bosshard, 1973), l-(Acyloxy)-lif-benzotriazoles or l-acyl-17f-benzo-triazole 3-oxides are formed as reactive intermediates. If carboxylic or phosphoric esters are to be formed from the acids and alcohols using DCC, 4-(pyrrolidin-l -yl)pyridine ( PPY A. Hassner, 1978 K.M. Patel, 1979) and HBT are efficient catalysts even with tert-alkyl, choles-teryl, aryl, and other unreactive alcohols as well as with highly bulky or labile acids. [Pg.145]


See other pages where Pyrrolidine-2-carboxylic acid esters, 3-hydroxy- from is mentioned: [Pg.136]    [Pg.340]    [Pg.136]    [Pg.454]    [Pg.126]    [Pg.108]    [Pg.101]   


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2- pyrrolidine-1 -carboxylate

Carboxylic esters from

Carboxylic pyrrolidine

Esters from carboxylic acids

From carboxylic acids

From hydroxy acids

From hydroxy esters

Hydroxy esters

Hydroxy esters from ester acids

Pyrrolidine acidity

Pyrrolidine-3-carboxylic acid

Pyrrolidines carboxylic acid

Pyrrolidines, 3-hydroxy— from

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