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

Creator:: Chadwick, Thomas Carl, 1945-
Resource Type:: Dissertation
Full Text:: ) are thought to proceed by the mechanism shown below (95, 202). H -CH2 39 OH Both cis -o-1, 3

The aromatic Cope rearrangement : energetics and reality

Creator:: Almond, Stephen W.
Resource Type:: Dissertation
Full Text:: AN ABSTRACT OF THE THESIS OF Stephen W. Almond for the degree of Doctor of Philosophy in Chemistry

The rate of alcoholysis of o-nitroacetanilide

Creator:: Nelson, Harry Martin
Resource Type:: Masters Thesis
Full Text:: / LITER) I o w 1.9 z w z'.8 -j z 4 o i.7 I- z ¿ 1.6 U. o z'.5 o U) U) jI.4 U

A reinvestigation of the Claisen rearrangement of allyl o-tolyl ether

Creator:: Richardson, Bruce Coburn
Resource Type:: Dissertation
Full Text:: A REINVESTIGATION OP THE CLAISEH REARRANGEMENT OP ALLYL o

A study of the Jacobsen rearrangement of 6-n-propyl-7-methyltetralin

Creator:: Olafsson, Patrick Gordon
Resource Type:: Dissertation
Full Text:: Arnold and darnes (1, o. 961). ihile this mechanism ac- counted for the necessity Lf having sulfuric

I. Isolation of certain toxic components of kraft mill waste and attempts to determine their structure. ; II. Studies of the mechanism of the cope rearrangement of 1,2-divinyl-1, 2-cyclohexanediol

Creator:: Banks, Richard Charles
Abstract:: PART I. A chemical examination of the materials toxic to fish in kraft pulp mill wastes has been made as part of a water pollution study. Thirty gallons of "foul condensate" from a typical kraft mill gave 14 g of organic material when extracted with methylene chloride, and an additional...
Resource Type:: Dissertation
Full Text:: unsaturated ketone contained 29 ± 6% Do, 39 ± 2% D 23 f 3% D2, and 7 f 1% D3 species. Each of these had the

The mechanism of the para-Claisen rearrangement

Creator:: Teranishi, Roy, 1922-2000
Resource Type:: Dissertation
Full Text:: -diallyl-4-('Y-phenylallyl)-phenol (compound 7). OH AA 5 O-A' 6 7 ii1 OH H ¿w O-A

The reaction of N-bromosuccinimide (I) with acetals

Creator:: Joncich, Micheal Joseph
Resource Type:: Masters Thesis
Full Text:: of the volatile o products, the acetal w distilled, b. p. 102 - 104 u.; fl20 1.3820; weiht 70.8

Some studies relating to the stereochemistry of the Claisen rearrangement of cis- and trans-α ,γ- dimethylallyl phenyl ethers

Creator:: Ong, Josephine
Resource Type:: Dissertation
Full Text:: - investigation of the Claisen rearrangement of cis - and trans -2- phenoxypent -3 -ene (OC (O( x -dimethylallyl

Isolation and identification of certain toxic compounds in a fraction of Kraft mill waste

Creator:: Wiman, Robert Edgar, 1933-
Resource Type:: Dissertation
Full Text:: Synthesis of 4- (p- tolyl) -1- 39 - (p- -valerolactone 39 4-(p-toly1)-pentanoic acid 40 Ethyl 4- (p

ScholarsArchive@OSU

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

The aromatic Cope rearrangement : energetics and reality

The rate of alcoholysis of o-nitroacetanilide

A reinvestigation of the Claisen rearrangement of allyl o-tolyl ether

A study of the Jacobsen rearrangement of 6-n-propyl-7-methyltetralin

I. Isolation of certain toxic components of kraft mill waste and attempts to determine their structure. ; II. Studies of the mechanism of the cope rearrangement of 1,2-divinyl-1, 2-cyclohexanediol

The mechanism of the para-Claisen rearrangement

The reaction of N-bromosuccinimide (I) with acetals

Some studies relating to the stereochemistry of the Claisen rearrangement of cis- and trans-α ,γ- dimethylallyl phenyl ethers

Isolation and identification of certain toxic compounds in a fraction of Kraft mill waste

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