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pubmed-article:3484361rdf:typepubmed:Citationlld:pubmed
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pubmed-article:3484361pubmed:issue5-6lld:pubmed
pubmed-article:3484361pubmed:dateCreated1988-4-25lld:pubmed
pubmed-article:3484361pubmed:abstractTextThe preparation of 6 beta-methoxy-7 alpha-bromoestradiol (1) is reported. Addition of in situ-generated BrOMe to 6-dehydroestradiol 3-tetrahydropyranyl ether (4a) afforded the expected addition product. Removal of the tetrahydropyranyl protective group was carried out by mild acid hydrolysis to afford 1 in good yields. This base-sensitive compound is chemically stable over long periods of time.lld:pubmed
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pubmed-article:3484361pubmed:statusMEDLINElld:pubmed
pubmed-article:3484361pubmed:issn0039-128Xlld:pubmed
pubmed-article:3484361pubmed:authorpubmed-author:MettlerF AFAlld:pubmed
pubmed-article:3484361pubmed:authorpubmed-author:HylaridesM...lld:pubmed
pubmed-article:3484361pubmed:authorpubmed-author:Nad'LLlld:pubmed
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pubmed-article:3484361pubmed:volume48lld:pubmed
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pubmed-article:3484361pubmed:pagination395-400lld:pubmed
pubmed-article:3484361pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:3484361pubmed:articleTitlePreparation of B-ring brominated derivatives of estradiol.lld:pubmed
pubmed-article:3484361pubmed:affiliationDepartment of Radiology, University of New Mexico, Albuquerque 87131.lld:pubmed
pubmed-article:3484361pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3484361pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed