Publication Number: WO/2002/079136 International Application No.: PCT/AU2002/000417 Publication Date: 10.10.2002 International Filing Date: 02.04.2002A method of forming a cyclopropane having enhanced chirality said method comprising reacting together (1), a symmetrical 1,2-dioxine of the formula (1), wherein X and Y are the same and are groups in which a carbon atom is bonded to the dioxine backbone; and a phosphorus ylide or a phosphorus ylide precursor; in the presence of a cobalt catalyst containing a chiral ligand
A stereoselective route to enantiomerically enriched bicyclic cyclopropane derivatives 13 is describ...
Thesis advisor: Xiaoxiang Peter ZhangThesis advisor: James P. MorkenDiazomalonates have been demonst...
Copyright © 2001 American Chemical SocietyThe bulky stabilized ylides (2a-d) react with a range of 1...
Copies of the author's previously published works inserted.Includes bibliographical references (leav...
A new method is described for the synthesis of diastereomerically pure cyclopropanes from substitute...
The development of new methodology for the asymmetric synthesis of chiral organic compounds is a ma...
Both physical and organic chemists are interested in the cyclopropane ring, the former owing to the ...
Cyclopropanation reactions using zinc carbenoids are a powerful means to access cyclopropanes. Descr...
A user-friendly, one-pot procedure was developed to access racemic as well as enantiomerically enric...
© The Royal Society of Chemistry 2002The combination of chiral cobalt β-ketoiminato or cobalt salen ...
Publication Number: WO/2003/031425 International Application No.: PCT/AU2002/001351 Publication Date...
Includes a copy of an article co-authored by the author during the preparation of this thesis.Includ...
This thesis is concerned with the asymmetric synthesis of cyclopropyl derivatives via the...
Metal-catalyzed cyclopropanation of olefins with diazo reagents has attracted research interest beca...
A new approach for the synthesis of diastereomerically pure cyclopropanes from 1,2-dioxines and ster...
A stereoselective route to enantiomerically enriched bicyclic cyclopropane derivatives 13 is describ...
Thesis advisor: Xiaoxiang Peter ZhangThesis advisor: James P. MorkenDiazomalonates have been demonst...
Copyright © 2001 American Chemical SocietyThe bulky stabilized ylides (2a-d) react with a range of 1...
Copies of the author's previously published works inserted.Includes bibliographical references (leav...
A new method is described for the synthesis of diastereomerically pure cyclopropanes from substitute...
The development of new methodology for the asymmetric synthesis of chiral organic compounds is a ma...
Both physical and organic chemists are interested in the cyclopropane ring, the former owing to the ...
Cyclopropanation reactions using zinc carbenoids are a powerful means to access cyclopropanes. Descr...
A user-friendly, one-pot procedure was developed to access racemic as well as enantiomerically enric...
© The Royal Society of Chemistry 2002The combination of chiral cobalt β-ketoiminato or cobalt salen ...
Publication Number: WO/2003/031425 International Application No.: PCT/AU2002/001351 Publication Date...
Includes a copy of an article co-authored by the author during the preparation of this thesis.Includ...
This thesis is concerned with the asymmetric synthesis of cyclopropyl derivatives via the...
Metal-catalyzed cyclopropanation of olefins with diazo reagents has attracted research interest beca...
A new approach for the synthesis of diastereomerically pure cyclopropanes from 1,2-dioxines and ster...
A stereoselective route to enantiomerically enriched bicyclic cyclopropane derivatives 13 is describ...
Thesis advisor: Xiaoxiang Peter ZhangThesis advisor: James P. MorkenDiazomalonates have been demonst...
Copyright © 2001 American Chemical SocietyThe bulky stabilized ylides (2a-d) react with a range of 1...