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Parker, Kathlyn A., Koh, Yung-hyo (1994) Methodology for the Regiospecific Synthesis of Bis C-Aryl Glycosides. Models for Kidamycins. Journal Of The American Chemical Society, 116 (24) 11149-11150 doi:10.1021/ja00103a037

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Reference TypeJournal (article/letter/editorial)
TitleMethodology for the Regiospecific Synthesis of Bis C-Aryl Glycosides. Models for Kidamycins
JournalJournal Of The American Chemical Society
AuthorsParker, Kathlyn A.Author
Koh, Yung-hyoAuthor
Year1994 (November)Volume116
Issue24
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00103a037Search in ResearchGate
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Mindat Ref. ID1483605Long-form Identifiermindat:1:5:1483605:3
GUID0
Full ReferenceParker, Kathlyn A., Koh, Yung-hyo (1994) Methodology for the Regiospecific Synthesis of Bis C-Aryl Glycosides. Models for Kidamycins. Journal Of The American Chemical Society, 116 (24) 11149-11150 doi:10.1021/ja00103a037
Plain TextParker, Kathlyn A., Koh, Yung-hyo (1994) Methodology for the Regiospecific Synthesis of Bis C-Aryl Glycosides. Models for Kidamycins. Journal Of The American Chemical Society, 116 (24) 11149-11150 doi:10.1021/ja00103a037
In(1994, November) Journal Of The American Chemical Society Vol. 116 (24) American Chemical Society (ACS)

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Parker, Kathlyn A., Coburn, Craig A. (1991) Reductive aromatization of quinol ketals: a new synthesis of C-aryl glycosides. Journal Of The American Chemical Society, 113 (22) 8516-8518 doi:10.1021/ja00022a046
Parker, Kathlyn A., Kallmerten, James (1980) Efficient, regiospecific synthesis of anthracycline intermediates: total synthesis of daunomycin. Journal Of The American Chemical Society, 102 (18) 5881-5886 doi:10.1021/ja00538a029
Parket, Kathlyn A., Coburn, Craig A. (1992) Reductive aromatization of quinol ketals: a new synthesis of C-aryl glycosides. [Erratum to document cited in CA115(19):208369c]. Journal Of The American Chemical Society, 114 (4) 1533 doi:10.1021/ja00030a089
Parker, Kathlyn A., Mindt, Thomas L., Koh, Yung-hyo (2006) TESOTf-Induced Rearrangement of Quinols. Efficient Construction of the Fully Functionalized Carbon Skeleton of the Griseusins by a Divergent−Reconvergent Approach. Organic Letters, 8. 1759-1762 doi:10.1021/ol060206q
Parker, Kathlyn A., Lim, Yeon-Hee (2004) The Total Synthesis of (−)-SNF4435 C and (+)-SNF4435 D. Journal Of The American Chemical Society, 126 (49) 15968-15969 doi:10.1021/ja044733l
Parker, Kathlyn A., Fokas, Demosthenes (1992) Convergent synthesis of (.+-.)-dihydroisocodeine in 11 steps by the tandem radical cyclization strategy. A formal total synthesis of (.+-.)-morphine. Journal Of The American Chemical Society, 114 (24) 9688-9689 doi:10.1021/ja00050a075
am Ende, Christopher W., Zhou, Zhou, Parker, Kathlyn A. (2013) Total Synthesis of (±)-Bisabosqual A. Journal Of The American Chemical Society, 135 (2) 582-585 doi:10.1021/ja3108577
Stork, Gilbert., Gardner, John O., Beckman, Robert K., Parker, Kathlyn A. (1973) Haloketal cyclization. General method for the synthesis of functionalized cis bicyclic ketones. Journal Of The American Chemical Society, 95 (6) 2014-2016 doi:10.1021/ja00787a052
Stien, Didier, Anderson, Glen T., Chase, Charles E., Koh, Yung-hyo, Weinreb, Steven M. (1999) Total Synthesis of the Antitumor Marine Sponge Alkaloid Agelastatin A. Journal Of The American Chemical Society, 121 (41) 9574-9579 doi:10.1021/ja992487l
Song, Airong, Parker, Kathlyn A., Sampson, Nicole S. (2009) Synthesis of Copolymers by Alternating ROMP (AROMP) Journal Of The American Chemical Society, 131 (10) 3444-3445 doi:10.1021/ja809661k
Lim, Hee Nam, Parker, Kathlyn A. (2011) Total Synthesis of the Potent Androgen Receptor Antagonist (−)-Arabilin: A Strategic, Biomimetic [1,7]-Hydrogen Shift. Journal Of The American Chemical Society, 133 (50) 20149-20151 doi:10.1021/ja209459f
 
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