Efficient, non-acidolytic method for the selective cleavage of N-Boc amino acid and peptide phenacyl esters linked to a polystyrene resin

被引:40
作者
Furlán, RLE [1 ]
Mata, EG [1 ]
Mascaretti, OA [1 ]
机构
[1] Univ Nacl Rosario, CONICET, Inst Quim Organ Sintesis, Fac Ciencias Bioquim & Farmaceut, RA-2000 Rosario, Argentina
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1998年 / 02期
关键词
D O I
10.1039/a704118g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient, non-acidolytic method for the selective cleavage of phenacyl esters of N-Boc-amino acids and -peptides linked to a polystyrene resin by (CH3)(3)SnOH (TMTOH) or [(n-C4H9)(3)Sn](2)O (BBTO) is described, We highly recommend the use of trimethyltin hydroxide for the selective cleavage of carboxylic esters based on its favourable properties, The method is compatible with an N-Boc/O-Bn (benzyl ether) strategy and yields enantiomerically pure N-Boc-peptides useful for further manipulation, for segment condensations or for cyclization strategies, A mechanism for the cleavage of methyl phenylacetate in solution by TMTOH is postulated.
引用
收藏
页码:355 / 358
页数:4
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