Photocleavable protecting groups as nucleobase protections allowed the solid-phase synthesis of base-sensitive SATE-prooligonucleotides

K Alvarez, JJ Vasseur, T Beltran…

Index: Journal of Organic Chemistry, , vol. 64, # 17 p. 6319 - 6328

Full Text: HTML

Citation Number: 51

Abstract

... The Journal of Organic Chemistry. ... Montpellier Cedex 5, France. J. Org. Chem. , 1999, 64 (17), pp 6319–6328. DOI: 10.1021/jo990479h. Publication Date (Web): August 3, 1999. Copyright © 1999 American Chemical Society. ...

Related Articles:

Oligonucleotide synthesis involving deprotection of amidine-type protecting groups for nucleobases under acidic conditions

[Organic Letters, , vol. 12, # 11 p. 2496 - 2499]

Synthesis of 2'-deoxytubercidin, 2'-deoxyadenosine, and related 2'-deoxynucleosides via a novel direct stereospecific sodium salt glycosylation procedure

[Journal of the American Chemical Society, , vol. 106, # 21 p. 6379 - 6382]

Smooth and efficient deoxygenation of secondary alcohols. A general procedure for the conversion of ribonucleosides to 2'-deoxynucleosides

[Journal of the American Chemical Society, , vol. 103, # 4 p. 932 - 933]

Smooth and efficient deoxygenation of secondary alcohols. A general procedure for the conversion of ribonucleosides to 2'-deoxynucleosides

[Journal of the American Chemical Society, , vol. 103, # 4 p. 932 - 933]

Improved procedure for the regiospecific synthesis of 2′-deoxyribonucleosides

[Tetrahedron Letters, , vol. 31, # 31 p. 4437 - 4440]

More Articles...