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ScharerDavid Orlando

Scharer, Orlando D.
Schärer Lab.
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dc.citation.endPage 4208 -
dc.citation.number 24 -
dc.citation.startPage 4205 -
dc.citation.title ORGANIC LETTERS -
dc.citation.volume 4 -
dc.contributor.author Gillet, Ludovic C. J. -
dc.contributor.author Scharer, Orlando D. -
dc.date.accessioned 2023-12-22T11:36:33Z -
dc.date.available 2023-12-22T11:36:33Z -
dc.date.created 2017-01-26 -
dc.date.issued 2002-11 -
dc.description.abstract C8-Amine and acetylamine adducts of 2'-deoxyguanosine were synthesized. Our approach provides solutions for the coupling of aromatic amines to a protected 8-bromo-2'-deoxyguanosine derivative, for the selective acetylation of the coupled adduct at N-8 and for a protecting group scheme preserving the integrity of the base-labile N-8 acetyl group during DNA synthesis. -
dc.identifier.bibliographicCitation ORGANIC LETTERS, v.4, no.24, pp.4205 - 4208 -
dc.identifier.doi 10.1021/ol026474f -
dc.identifier.issn 1523-7060 -
dc.identifier.scopusid 2-s2.0-0037191621 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/21290 -
dc.identifier.url http://pubs.acs.org/doi/abs/10.1021/ol026474f -
dc.identifier.wosid 000179430600006 -
dc.language 영어 -
dc.publisher AMER CHEMICAL SOC -
dc.title Preparation of C8-amine and acetylamine adducts of 2 '-deoxyguanosine suitably protected for DNA synthesis -
dc.type Article -
dc.description.journalRegisteredClass scopus -

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