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Protection of 5′‐Hydroxy Functions of Nucleosides
dc.contributor.authorSeliger, H.
dc.date.accessioned2018-05-15T20:15:04Z
dc.date.available2018-05-15T20:15:04Z
dc.date.issued2000-02
dc.identifier.citationSeliger, H. (2000). "Protection of 5′‐Hydroxy Functions of Nucleosides." Current Protocols in Nucleic Acid Chemistry 00(1): 2.3.1-2.3.34.
dc.identifier.issn1934-9270
dc.identifier.issn1934-9289
dc.identifier.urihttps://hdl.handle.net/2027.42/143732
dc.description.abstractThe 5‐hydroxy group is the primary hydroxy group of nucleosides. It is mandatory to protect 5‐hydroxyls in all methods of oligonucleotide synthesis that require nucleoside synthons. This unit discusses a wide variety of acid‐labile and base‐labile protecting groups, as well as enzymatic methods for 5‐protection and deprotection.
dc.publisherIRL Press
dc.publisherWiley Periodicals, Inc.
dc.titleProtection of 5′‐Hydroxy Functions of Nucleosides
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelBiological Chemistry
dc.subject.hlbsecondlevelChemical Engineering
dc.subject.hlbsecondlevelPublic Health
dc.subject.hlbsecondlevelChemistry
dc.subject.hlbtoplevelScience
dc.subject.hlbtoplevelEngineering
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/143732/1/cpnc0203.pdf
dc.identifier.doi10.1002/0471142700.nc0203s00
dc.identifier.sourceCurrent Protocols in Nucleic Acid Chemistry
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