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Stereocontrol with 2-oxazolinesBower, Justin F. January 1996 (has links)
No description available.
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Studies directed towards the total synthesis of the natural product diazonamide AKreisberg, Jennifer Diane. January 2001 (has links)
Thesis (Ph. D.)--University of Texas at Austin, 2001. / Vita. Includes bibliographical references. Available also from UMI/Dissertation Abstracts International.
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Studies directed towards the total synthesis of the natural product diazonamide A /Kreisberg, Jennifer Diane, January 2001 (has links)
Thesis (Ph. D.)--University of Texas at Austin, 2001. / Vita. Includes bibliographical reference. Available also in a digital version from Dissertation Abstracts.
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Studies directed towards the total synthesis of the natural product diazonamide AKreisberg, Jennifer Diane 23 March 2011 (has links)
Not available / text
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The absolute configuration of streptidine in streptomycinTodd, Aaron William 08 1900 (has links)
No description available.
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Stereochemistry of cobalt (III) complexes of trans-1,2-cyclopentanediaminePhillips, John Francis 08 1900 (has links)
No description available.
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Complexes of cobalt (III) with trans-1,2-cyclopentanediamineCross, Wendall Hugh 12 1900 (has links)
No description available.
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The isomerization and stereochemistry of some iridium hydride complexes /Yorke, William John. January 1979 (has links)
Samples of fac and mer carbonyltrihydridotris(triphenylphosphine)iridium (III) were prepared and fully characterized by i.r., ('1)H and ('31)P n.m.r. spectroscopies. Isomeric interconversion at 25(DEGREES) C was demonstrated. The rates of isomerization and hydrogen loss from each isomer were independently measured. The similarity of these rates strongly supports a mechanism by which isomerization occurs through the oxidative addition and reductive elimination of molecular hydrogen. The results of deuterium labelling experiments were consistent with the isomerization mechanism, and further suggest that either trans-oxidative addition of hydrogen or intramolecular hydride interchange in the mer isomer may occur. Various partially deuterated analogues of the fac and mer isomer were formed by further reaction in solution and identified in the ('1)H n.m.r. spectrum. An unusual downfield isotope shift occurred when deuterium is in a position trans to hydride.
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The structure, stereochemistry and reactions of [beta]-isocamphorJudd, Claude Ivan, January 1957 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1957. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 66-68).
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Synthetic approaches to the yohimbine systemKnapp, Gordon Grayson, January 1956 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1956. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves [92-93]).
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