Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
1982-2-12
pubmed:abstractText
The synthesis of the self-complementary decadeoxynucleotide d(AATTGCAATT) is described. The phosphotriester method has been used with several modifications. Protected nucleotides have been prepared in a one-step reaction involving a new monofunctional phosphorylating agent: p-chlorophenyl-beta-cyanoethyl phosphate. Triethylammonium salts of mononucleoside 3'-phosphodiesters were obtained either by decyanoethylation of the triesters or, in the case of thymine, by a one-step reaction starting from 5'-0-methoxytritylthymidine and the mixture pyridine-para-chlorophenyl-methyl-phosphorobromidate. The usual coupling reactions were then used to prepare the decadeoxynucleotide in large quantities.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0300-9084
pubmed:author
pubmed:issnType
Print
pubmed:volume
63
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
775-84
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed:year
1981
pubmed:articleTitle
Synthesis and structural studies of a self-complementary decadeoxynucleotide d(AATTGCAATT). I.-Synthesis and chemical characterization of the decanucleotide.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't