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Preparation and decomposition of C-14 labeled Mannich base

Creator:: Dorward, Donald Lyle
Resource Type:: Masters Thesis
Full Text:: of the Chemical Society, 6 79-Sl 6. Lieberten, $. V, end Wagner, !;, C, "The course of the

Addition of hydrogen bromide to unsymmetrical olefins

Creator:: Rogers, Charles Junior
Abstract:: In this investigation the addition of hydrogen bromide to 3-methylcyclohexene has been studied in order to see if the theory of hyperconjugation could be extended to include olefins of this type. Since the olefin has an equal number of hydrogens on both carbons carrying the double bond, a mixture of...
Resource Type:: Dissertation
Full Text:: hydrogen bromide was conducted at 0°C and at room temperature using glacial acetic acid as a solvent. The

The preparation and reactions of 1-(2-pyridyl)-3-menthyl-3-butene-2-ol and 1-(2-pyridyl)-4-methyl-3-butene-2-ol

Creator:: Janposri, Sompong
Abstract:: 1-(2-pyridyl)-3-methyl-3-butene-2-ol was prepared by allowing 2-picolyllithium to react with methacrolein. In the reaction of picolyllithium with crotonaldehyde, two products 1-(2-pyridyl)-4-methyl-3-butene-2-ol and 1-(2-pyridyl)-4-methyl-2-butene-4-ol were formed. 1-(2-pyridyl)-3-methyl-3-butene-2-ol was subjected to the low pressure hydrogenation, using methanol as solvent and PtO₂ as catalyst. A red yellow liquid 1-(2-pyridyl)-3-methyl-2-butanol was obtained. Derivatives of the...
Resource Type:: Masters Thesis
Full Text:: . V. spectrum. 3. The compound 1 -(2-pyridyl)-3-me thyl-3-butene-2-ol "V N* CH -CH- C =CH, 2 i i 2

Reactions of 1-phenyl-4-(2-pyridyl)-1-butene-3-ol

Creator:: Pojanagaroon, Pairoje
Resource Type:: Masters Thesis
Full Text:: C6H5 Compound V 9 OH CH2-CH-CH = CH HC1 ( solid) O NÌ O-C 1 H2-CH-CH = CH Compound

Addition reactions of the condensate of picolyllithium and certain unsaturated aldehydes

Creator:: Wischmann, Kenneth Brandt
Resource Type:: Masters Thesis
Full Text:: author wishes to express his sincere thanks to Dr. Albert V. Logan for his guidance and. help during

Reactions of the condensates of picolyllithium and acrolein

Creator:: Arthachinta, Sukanda
Resource Type:: Masters Thesis
Full Text:: to express her deep gratitude to Dr. A. V. Logan for his valuable advice and his encourage- ment

Reactions of the condensates of picolyllithium and acrolein and methacrolein

Creator:: Nash, Boyd D.
Resource Type:: Masters Thesis
Full Text:: -------- C6H5CHCF{CHOJICH2R V - 2-pyridyl, 4-pyridyl, or 5-methyl-2-pyridyl C6H5CHCHCHCHR VI More recently

Reactions of I-(α-pyridyl)-3-buten-1-o1

Creator:: Whitman, James Edgar
Abstract:: The purpose of this project was to study the reactions of 1-(α-pyridyl)-3-buten-1-ol (compound I) and to determine whether or not the products of some of its reactions are quinolizinium salts. Reaction of compound I with bromine or iodine yields halide salts (when no external cooling is applied) instead of the...
Resource Type:: Masters Thesis
Full Text:: , 34.76:, H, 4,2L. Found: C, 34.79; H, 4.37. 1 -(o-pyridyl) -3-brornobutanol (cornpound V): Excess

Applications of the Mannich reaction

Creator:: Bush, David Clair
Resource Type:: Dissertation
Full Text:: , 1942. pp.303-341. 7. Burrus, Harry O. and C-arfield Powell. Amines related to epinephrine. V

The Robinson-Mannich base synthesis applied to substituted acetoacetic ester

Creator:: LaPore, Richard Francis
Resource Type:: Dissertation
Full Text:: -doctoral fellowship . Gx-atef'ul thanks are also e;xtended to DP. Albert V.. Logan :for his guidance

ScholarsArchive@OSU

Preparation and decomposition of C-14 labeled Mannich base

Addition of hydrogen bromide to unsymmetrical olefins

The preparation and reactions of 1-(2-pyridyl)-3-menthyl-3-butene-2-ol and 1-(2-pyridyl)-4-methyl-3-butene-2-ol

Reactions of 1-phenyl-4-(2-pyridyl)-1-butene-3-ol

Addition reactions of the condensate of picolyllithium and certain unsaturated aldehydes

Reactions of the condensates of picolyllithium and acrolein

Reactions of the condensates of picolyllithium and acrolein and methacrolein

Reactions of I-(α-pyridyl)-3-buten-1-o1

Applications of the Mannich reaction

The Robinson-Mannich base synthesis applied to substituted acetoacetic ester

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