Nucleic-acid analogs with constraint conformational flexibility in the sugar-phosphate backbone "Tricyclo-DNA". Part 1. Preparation of [(5'R,6'R)-2-deoxy-3',5'-ethano-5',6'-methano-beta-D-ribofuranosyl]thymine and -adenine, and the corresponding phosphoramidites for oligonucleotide synthesis

Steffens, R.; Leumann, Christian (1997). Nucleic-acid analogs with constraint conformational flexibility in the sugar-phosphate backbone "Tricyclo-DNA". Part 1. Preparation of [(5'R,6'R)-2-deoxy-3',5'-ethano-5',6'-methano-beta-D-ribofuranosyl]thymine and -adenine, and the corresponding phosphoramidites for oligonucleotide synthesis. Helvetica chimica acta, 80(8), pp. 2426-2439. Verlag Helvetica Chimica Acta 10.1002/hlca.19970800812

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Item Type:

Journal Article (Original Article)

Division/Institute:

08 Faculty of Science > Departement of Chemistry and Biochemistry

UniBE Contributor:

Leumann, Christian

Subjects:

500 Science > 570 Life sciences; biology
500 Science > 540 Chemistry

ISSN:

0018-019X

Publisher:

Verlag Helvetica Chimica Acta

Language:

English

Submitter:

Christian Leumann

Date Deposited:

20 May 2015 14:34

Last Modified:

20 May 2015 14:34

Publisher DOI:

10.1002/hlca.19970800812

Uncontrolled Keywords:

adenine analog ANALOGS backbone NUCLEIC-ACID ANALOGS oligonucleotide phosphoramidite SUGAR-PHOSPHATE BACKBONE synthesis

BORIS DOI:

10.7892/boris.68615

URI:

https://boris.unibe.ch/id/eprint/68615

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