Gelation Behavior of 2H-Chromene N-Acylamino Acid Conjugates
摘要:
[GRAPHICS]2H-Chromene-based conjugates of N-acyl-1,omega-amino acids (5, 9a-f, 14a-f) of natural amino acids (10a,b) and of dipeptide (10c) are prepared (60-97%) by N-acylbenzotriazole methodology in aqueous media at 20 degrees C. Gelation properties of the corresponding sodium salts in DMF and DMSO are generalized with respect to an increase or decrease in the chain length of the spacer.
Gelation Behavior of 2H-Chromene N-Acylamino Acid Conjugates
摘要:
[GRAPHICS]2H-Chromene-based conjugates of N-acyl-1,omega-amino acids (5, 9a-f, 14a-f) of natural amino acids (10a,b) and of dipeptide (10c) are prepared (60-97%) by N-acylbenzotriazole methodology in aqueous media at 20 degrees C. Gelation properties of the corresponding sodium salts in DMF and DMSO are generalized with respect to an increase or decrease in the chain length of the spacer.
Gelation Behavior of 2<i>H</i>-Chromene <i>N</i>-Acylamino Acid Conjugates
作者:Alan R. Katritzky、Rajeev Sakhuja、Levan Khelashvili、Karem Shanab
DOI:10.1021/jo900066m
日期:2009.4.17
[GRAPHICS]2H-Chromene-based conjugates of N-acyl-1,omega-amino acids (5, 9a-f, 14a-f) of natural amino acids (10a,b) and of dipeptide (10c) are prepared (60-97%) by N-acylbenzotriazole methodology in aqueous media at 20 degrees C. Gelation properties of the corresponding sodium salts in DMF and DMSO are generalized with respect to an increase or decrease in the chain length of the spacer.