A new method is described for the synthesis of diastereomerically pure cyclopropanes from substituted 1,2-dioxines 1a–c and stabilised phosphorus ylides 2a–e.Thomas D. Avery, Thomas D. Haselgrove, Dennis K. Taylor, Edward R. T. Tiekink and Tanya J. Rathbon
This Thesis is focused on the preparation of organic molecules that contain a three-membered ring sy...
The cyclopropane moiety is found in a wide variety of the natural products, from small amino acid mo...
The stereoselective preparation of three stereoisomeric tercyclopropanes and a quinquecyclopropane w...
A new approach for the synthesis of diastereomerically pure cyclopropanes from 1,2-dioxines and ster...
Copies of the author's previously published works inserted.Includes bibliographical references (leav...
Addition of stabilized Horner-Wadsworth-Emmons (HWE) phosphonates to substituted 1,2-dioxines leads ...
Copyright © 2001 American Chemical SocietyThe bulky stabilized ylides (2a-d) react with a range of 1...
Includes a copy of an article co-authored by the author during the preparation of this thesis.Includ...
The reaction of aryl- and vinyl-stabilized sulfonium ylides with electron-poor dienes has been inves...
Publication Number: WO/2002/079136 International Application No.: PCT/AU2002/000417 Publication Date...
l,2-Dioxines are an important class of compounds that are useful in organic synthesis for the incorp...
The identification of two natural products, FR-900848 and U-106305, has stimulated interest concerni...
The diastereoselective cyclopropanation of three stereoisomerically unique vinylcyclopropanes was st...
A highly diastereoselective cyclopropanation of cyclic enones with sulfur ylides was developed under...
Diastereoselective cyclopropanation of a trans-substituted vinyl cyclopropane was studied. The stere...
This Thesis is focused on the preparation of organic molecules that contain a three-membered ring sy...
The cyclopropane moiety is found in a wide variety of the natural products, from small amino acid mo...
The stereoselective preparation of three stereoisomeric tercyclopropanes and a quinquecyclopropane w...
A new approach for the synthesis of diastereomerically pure cyclopropanes from 1,2-dioxines and ster...
Copies of the author's previously published works inserted.Includes bibliographical references (leav...
Addition of stabilized Horner-Wadsworth-Emmons (HWE) phosphonates to substituted 1,2-dioxines leads ...
Copyright © 2001 American Chemical SocietyThe bulky stabilized ylides (2a-d) react with a range of 1...
Includes a copy of an article co-authored by the author during the preparation of this thesis.Includ...
The reaction of aryl- and vinyl-stabilized sulfonium ylides with electron-poor dienes has been inves...
Publication Number: WO/2002/079136 International Application No.: PCT/AU2002/000417 Publication Date...
l,2-Dioxines are an important class of compounds that are useful in organic synthesis for the incorp...
The identification of two natural products, FR-900848 and U-106305, has stimulated interest concerni...
The diastereoselective cyclopropanation of three stereoisomerically unique vinylcyclopropanes was st...
A highly diastereoselective cyclopropanation of cyclic enones with sulfur ylides was developed under...
Diastereoselective cyclopropanation of a trans-substituted vinyl cyclopropane was studied. The stere...
This Thesis is focused on the preparation of organic molecules that contain a three-membered ring sy...
The cyclopropane moiety is found in a wide variety of the natural products, from small amino acid mo...
The stereoselective preparation of three stereoisomeric tercyclopropanes and a quinquecyclopropane w...