A reagent for the efficient cleavage of N-benzoylhomoserine lactones: Access to α-(2-phenylseleno)ethyl amino acids
作者:Michelle L. Pedersen、David B. Berkowitz
DOI:10.1016/s0040-4039(00)60175-2
日期:1992.11
diselenide and sodium trimethoxyborohydride (1:2) in DMF to 60°C, a reagent is produced which efficiently cleaves α-substituted N-benzoylhomoserine lactones to the corresponding α-(2-phenylseleno)ethyl amino acids without competing lactone reduction.
将二苯基二硒化物和三甲氧基硼氢化钠(1:2)在DMF中加热到60°C后,制得的试剂可有效地将α-取代的N-苯甲酰基高丝氨酸内酯裂解为相应的α-(2-苯基硒代)乙基氨基酸,而不会发生内酯还原反应。