Enantioselective synthesis and application of the highly fluorescent and environment-sensitive amino acid 6-(2-dimethylaminonaphthoyl) alanine (DANA)Electronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b2/b205224e/
摘要:
6-(2-二甲氨基萘酰基)丙氨酸 (DANA) 通过对映选择性合成制备,并掺入 RNase S 的 S 肽中,从而在肽-蛋白质相互作用时产生荧光的巨大变化。
Enantioselective synthesis and application of the highly fluorescent and environment-sensitive amino acid 6-(2-dimethylaminonaphthoyl) alanine (DANA)Electronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b2/b205224e/
摘要:
6-(2-二甲氨基萘酰基)丙氨酸 (DANA) 通过对映选择性合成制备,并掺入 RNase S 的 S 肽中,从而在肽-蛋白质相互作用时产生荧光的巨大变化。
A facile protocol for the convenient preparation of amino-substituted α-bromo- and α,α-dibromo arylmethylketones
作者:Zhenjun Diwu、Christopher Beachdel、Dieter H. Klaubert
DOI:10.1016/s0040-4039(98)00975-7
日期:1998.7
Amino-substituted arylmethylketones are selectively brominated in sulfuric acid to afford the corresponding dibromomethylarylketones that are then debrominated with diethylphosphite to give the desired bromomethylarylketones in excellent yield. (C) 1998 Published by Elsevier Science Ltd. All rights reserved.