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Decarboxylation studies on α-methyl-α-Phenylcaproic acid and some of its derivatives

Creator:: Sheppard, Dorothy Louise
Resource Type:: Masters Thesis
Full Text:: $t gs-og e(=!{gtby!--ot:#beg3rl-- - saprglg $c!d-_agd._$gng gf-r&e-Dgrlvgtlvgor- - Abstract approved

Pyrolysis of diterminally unsaturated, eight-member chains

Creator:: Fleming, Michael Paul
Resource Type:: Masters Thesis
Full Text:: ). 34. H. Pines and N. E. Hoffman, J. Amer. Chem. Soc., 76, 4417 (1954). 49 35. W. D. Huntsman and T

Thermal valence isomerization of trienes

Creator:: Polston, Norman Lee
Resource Type:: Masters Thesis
Full Text:: - hexatrienes from bromohexadienes by quaternization with an amine followed by Hoffman elimination ac

Thermolysis of cis,cis,trans-1-phenyl-1,3,5-heptatriene

Creator:: Tilton, Mary Lehman
Abstract:: Isomerically pure cis,cis,trans-1-pheny1-1,3,5- heptatriene was prepared and cyclized. Ring closure was followed by a 1,5 hydrogen shift, and the only product observed was 1-phenyl -6-methyl -1,3-cyclohexadiene. Rough first order rate constants for thermolysis and the hydrogen shift were determined. Kinetic estimates indicate that the report of disallowed product in a...
Resource Type:: Masters Thesis
Full Text:: -202° 29 (lit. (25) mp 200-202°); nmr (CC14) 67.34-7.74 (m, 5H, C6H5), 5.56 (d, 1H, J = 12 Hz

Part I. Synthesis and Cope rearrangement of some substituted hexadienes. Part II. Formation of N-phenyl and N-methyl pyridinium salts from 1, 7-diaza-1, 3, 5-heptatrienes

Creator:: Li, Thomas Hoi-chow
Resource Type:: Dissertation
Full Text:: . ) Page 1-(p-Bromopheny1)-4-penten-l-one (67-f) 96 1-(p-Chloropheny1)-4-penten-l-one (67-d) 96 1-(p-toly1

The aromatic Cope rearrangement : energetics and reality

Creator:: Almond, Stephen W.
Resource Type:: Dissertation
Full Text:: by Opal Grossnicklaus for Stephen W. Almond To G. D. ACKNOWLEDGEMENTS The author is grateful

The synthesis and valence isomerization of some para-substituted 1-phenyl-1,3,5-hexatrienes

Creator:: Platt, James LeGrande
Resource Type:: Dissertation
Full Text:: hybridization. a7//d b a (4) Assuming the principle of least motion for this isomerization the four carbons

The retro-ene reaction of 2-vinylcyclohexanols and approaches to the synthesis of botryococcene

Creator:: Rusay, Ronald Joseph
Abstract:: The retro-ene reaction of 2-vinylcyclohexanols occurs readily in the vapor phase at 400-450° producing unsaturated carbonyl compounds in good yields. The starting- materials were prepared in general by the carbenoid addition reaction of ethyl diazoacetate, appropriately substituted cyclohexene, and copper catalyst to produce bicyclic esters which were reduced to the...
Resource Type:: Dissertation
Full Text:: -Hoffman rules for cycloadditions, but the reaction is also highly sensitive to steric effects. A number

1,2-divinylcyclohexenes : synthesis and thermal rearrangement studies

Creator:: Delphey, Craig Edward
Resource Type:: Dissertation
Full Text:: occur. Inhoffen (83) found an anomalous side reaction during his work with models of the vitamin D

The kinetics and stereochemistry of electrocyclic ring cleavage of some 2H-pyrans

Creator:: Chadwick, Thomas Carl, 1945-
Resource Type:: Dissertation
Full Text:: such as D, L-cannabichromene, franklinone, a.11oevodionol, evodionol methyl ether, flemigen C

ScholarsArchive@OSU

Decarboxylation studies on α-methyl-α-Phenylcaproic acid and some of its derivatives

Pyrolysis of diterminally unsaturated, eight-member chains

Thermal valence isomerization of trienes

Thermolysis of cis,cis,trans-1-phenyl-1,3,5-heptatriene

Part I. Synthesis and Cope rearrangement of some substituted hexadienes. Part II. Formation of N-phenyl and N-methyl pyridinium salts from 1, 7-diaza-1, 3, 5-heptatrienes

The aromatic Cope rearrangement : energetics and reality

The synthesis and valence isomerization of some para-substituted 1-phenyl-1,3,5-hexatrienes

The retro-ene reaction of 2-vinylcyclohexanols and approaches to the synthesis of botryococcene

1,2-divinylcyclohexenes : synthesis and thermal rearrangement studies

The kinetics and stereochemistry of electrocyclic ring cleavage of some 2H-pyrans

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