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rdf:type |
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lifeskim:mentions |
umls-concept:C0000263,
umls-concept:C0011516,
umls-concept:C0028948,
umls-concept:C0205145,
umls-concept:C0220781,
umls-concept:C0243126,
umls-concept:C0332256,
umls-concept:C0449445,
umls-concept:C0524637,
umls-concept:C1527240,
umls-concept:C1883254
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pubmed:issue |
12
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pubmed:dateCreated |
1988-8-11
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pubmed:abstractText |
A protected 2-aminopurine nucleoside suitable for incorporation into oligodeoxynucleotides using phosphite triester chemical synthesis procedures has been prepared via oxidation of a purine hydrazino derivative with silver (I) oxide. Five oligodeoxynucleotides containing Eco RI and Bam HI recognition sites have been prepared such that, in the double stranded form, the 2-aminopurine base has either a complementary thymine or cytosine nucleobase. The helix character and thermodynamic parameters for helix formation have been examined.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-1062791,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-2825124,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-2827747,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-2948952,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-2950238,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3001656,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3008089,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3010238,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3011780,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3011781,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3018674,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-319000,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-333399,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3456600,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3459152,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3461441,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-3553959,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-386283,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-393830,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-4016102,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-4281196,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-4811220,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-5767305,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-5891460,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-6096813,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-6224136,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-6261793,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-6291587,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-6728676,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-6824629,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-691058,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-7255177,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-7288,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2838824-866187
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0305-1048
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:day |
24
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5631-44
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
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pubmed:year |
1988
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pubmed:articleTitle |
A new approach to the synthesis of a protected 2-aminopurine derivative and its incorporation into oligodeoxynucleotides containing the Eco RI and Bam HI recognition sites.
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pubmed:affiliation |
Department of Chemistry, Boston College, Chestnut Hill, MA 02167.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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