Back to search
The isopropoxyacetic group for convenient base protection during solid-support synthesis of oligodeoxyribonucleotides and their triester analogs
Data up to Jan 2025
Published1989
Citations34
References3
Total Citations Per Year
Abstract
References (3)
The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups
1987 • 197 citations
Nucleotide chemistry. XX. Phosphite coupling procedure for generating internucleotide links
1975 • 146 citations
Alkyl phosphotriester modified oligodeoxyribonucleotides. V. Synthesis and absolute configuration ofRpandSpdiastereomers of an ethyl phosphotriester (Et) modifiedEcoRI recognition sequence, d[GGAA(Et)TTCC]. A synthetic approach to regio- and stereospecific ethylation-interference studies
1986 • 49 citations
Cited By (0)
No citing papers found in database