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The selective oxidation of organic compounds particularly by iodic acid

Creator:: Woods, Melford Allan
Resource Type:: Masters Thesis
Full Text:: .1ztnf o1utione were uaed &n he udy of the prtM1 octdation of organ&c corn'oun. The extent of

The nutritional requirements of Trichophyton interdigitale

Creator:: Mosher, William Allison
Resource Type:: Masters Thesis
Full Text:: organism s the spores of Trichophyton interdigitale are killed at 56°C. in 10 minutes. Lower

Electric moment studies of a series of related hydrazine derivates

Creator:: Frey, Paul Reheard
Resource Type:: Dissertation
Full Text:: STUDIES OF A SERIES OF RELATED HDRAZINE DERIVATIVES by PAUL REdEARD FREY A ÍEiESIS submitted

Stereoselective synthesis & application of enantioenriched main group α-haloalkyl organometal reagents

Creator:: Emerson, Christopher R.
Abstract:: Sulfoxide-ligand exchange (SLE) and asymmetric halogen-metal exchange (AHME) processes were separately examined for the enantioselective synthesis of functionalized alpha-haloalkylmetal (carbenoid) reagents. Carbenoids derived from SLE were used to effect stereospecific reagent-controlled homologation (StReCH) of boronic esters and those generated via AHME were engaged in Darzens-type chemistry with aldehydes. Abstract for...
Resource Type:: Dissertation
Full Text:: -/-")%#-$)(.#0+5/)-+6$%72++ !89/'%/':,'+;$#/<#-"&?+ + 1@&"$/("+/22$%*#0A+ + B/7'+>?+C

A study of the diffusion velocity of ovalbumin

Creator:: Ray, Billy Roger
Resource Type:: Masters Thesis
Full Text:: . Deteriination of the Cell Constants 43 IV. Deter:ination of trìe Diffusion Velocity of Ovalburnin at 4°C. 44

Catalytic desymmetrization of D₂d̳-symmertic proprochiral tetrasubstituted biphenyl compounds: a novel approach to the synthesis of axially chiral C₂-symmetric molecules

Creator:: Gunderson, Jeremey Tyson
Abstract:: Many D2d-symmetric 2,2',6,6'-tetrasubstituted biphenyls are readily prepared via net oxidative dimerization of appropriate 1,3-disubstituted benzenes. Conversion of such proprochiral compounds to useful C2-symmetric chiral biphenyls requires formal replacement of two substituents on opposing aryl ring units with alternate groups. This under exploited desymmetrization tactic has been demonstrated for the generation...
Resource Type:: Masters Thesis
Full Text:: Abstract approved: Paul R. Blakemore Many D2d-symmetric 2,2',6,6'-tetrasubstituted biphenyls are

Stereospecific Synthesis of Stereotriad Motifs and Alkenes Using Enantioenriched sp³-Hybridized Carbenoids

Creator:: Xun, Sun
Abstract:: Enantioenriched sp³-hybridized carbenoid reagents CR1R2MX (X = nucleofuge, M = electrofuge) of different types were investigated for the synthesis of polysubstituted alkyl chains by iterative stereospecific reagent-controlled homologation (StReCH) and for the stereospecific connective synthesis of alkenes by eliminative cross-coupling. In the first part, putative enantioenriched α-chloroalkyllithiums (CHRLiCl) were employed...
Resource Type:: Dissertation
Full Text:: : ______________________________________________________ Paul R. Blakemore Enantioenriched sp3-hybridized carbenoid reagents CR1R2MX (X

Precursor-directed Biosynthesis and Total Synthesis of Aniline-containing Natural Products from the Endophytic Fungus Chalara sp. 6661

Creator:: Khoshbakht, Mahsa
Abstract:: Chalaniline A, an unusual xanthone-like aminofulvene with modest cytotoxicity, and chalaniline B [1-anilino-2,8-dihydroxy-3-(hydroxymethyl)xanthone], an antibacterial aminoxanthone, were previously isolated by Loesgen and coworkers from vorinostat-treated Chalara sp. 6661. Of note, the anilino moiety found within both chalaniline structures originates from biotransformation of the HDAC inhibitor vorinostat (SAHA, suberanilohydroxamic acid) by...
Resource Type:: Dissertation
Full Text:: Endophytic Fungus Chalara sp. 6661 Abstract approved: Paul R. Blakemore Chalaniline A, an

A micro study of the reduction of organic hydroxyl compounds with hydriodic acid

Creator:: Mitchell, Herschel K.
Resource Type:: Masters Thesis
Full Text:: author wisheB to express his sincere apprec- iation to Dr. Roger J. Williams for helpful advice and

The ionization constant of pantothenic acid

Creator:: Moser, Robin Emerson
Resource Type:: Masters Thesis
Full Text:: [k.iiJ r,) 2 'ç . '1 (i) which, LI is the no1a1ity of the undisociated acid, d the other syibo1s

ScholarsArchive@OSU

The selective oxidation of organic compounds particularly by iodic acid

The nutritional requirements of Trichophyton interdigitale

Electric moment studies of a series of related hydrazine derivates

Stereoselective synthesis & application of enantioenriched main group α-haloalkyl organometal reagents

A study of the diffusion velocity of ovalbumin

Catalytic desymmetrization of D₂d̳-symmertic proprochiral tetrasubstituted biphenyl compounds: a novel approach to the synthesis of axially chiral C₂-symmetric molecules

Stereospecific Synthesis of Stereotriad Motifs and Alkenes Using Enantioenriched sp³-Hybridized Carbenoids

Precursor-directed Biosynthesis and Total Synthesis of Aniline-containing Natural Products from the Endophytic Fungus Chalara sp. 6661

A micro study of the reduction of organic hydroxyl compounds with hydriodic acid

The ionization constant of pantothenic acid

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