A simple stereoselective synthesis of ethyl (4Z)-4-cyanoalk-4-enoates via the Johnson-Claisen rearrangement of 3-hydroxy-2-methylenealkanenitriles is described
148 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1987.The product stereoselectivity...
An efficient, stereoselective synthesis of 4′-Ed4T is demonstrated. The synthesis is highlighted by ...
Acid-catalysed thermal rearrangement of 4-aryl-4-methylhex-5-en-2-ones (products of the Claisen rear...
An unprecedented stereochemical reversal from alkyl to aryl substituents in the Johnson-Claisen rear...
Johnson-Claisen rearrangement of the Baylis-Hillman adducts has been reported by Basavaiah and co-wo...
A practical entry into delta-ethoxycarbonyl-alpha,beta-unsaturated nitrites is described. alpha,beta...
The Johnson-Claisen rearrangement is a valuable method for the formation of new carbon-carbon bonds,...
Iridium(I)-catalyzed olefin isomerization in bis(allyl) ethers is integrated into a generally applic...
ABSTRACT: A dianionic Ireland−Claisen rearrangement of chiral, nonracemic α-methyl-β-hydroxy allylic...
This thesis is divided into five chapters. Chapter 1 is a review of de-aromatisation processes achie...
A new and general strategy for hetero- and carbocycle synthesis has been developed. The n-membered m...
The synthesis and Claisen rearrangement of methyl γ-aryloxycrotonates have been reinvestigated. A nu...
The synthesis of the isoquinuclidine core of the Iboga alkaloid family is described. This building b...
Progress was made towards the investigation of the stereochemical effects of Ireland-Claisen rearran...
Reaction of Grignard reagents with methyl 3-acetoxy-2-methylenealkanoates produces (2E)-2-substitute...
148 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1987.The product stereoselectivity...
An efficient, stereoselective synthesis of 4′-Ed4T is demonstrated. The synthesis is highlighted by ...
Acid-catalysed thermal rearrangement of 4-aryl-4-methylhex-5-en-2-ones (products of the Claisen rear...
An unprecedented stereochemical reversal from alkyl to aryl substituents in the Johnson-Claisen rear...
Johnson-Claisen rearrangement of the Baylis-Hillman adducts has been reported by Basavaiah and co-wo...
A practical entry into delta-ethoxycarbonyl-alpha,beta-unsaturated nitrites is described. alpha,beta...
The Johnson-Claisen rearrangement is a valuable method for the formation of new carbon-carbon bonds,...
Iridium(I)-catalyzed olefin isomerization in bis(allyl) ethers is integrated into a generally applic...
ABSTRACT: A dianionic Ireland−Claisen rearrangement of chiral, nonracemic α-methyl-β-hydroxy allylic...
This thesis is divided into five chapters. Chapter 1 is a review of de-aromatisation processes achie...
A new and general strategy for hetero- and carbocycle synthesis has been developed. The n-membered m...
The synthesis and Claisen rearrangement of methyl γ-aryloxycrotonates have been reinvestigated. A nu...
The synthesis of the isoquinuclidine core of the Iboga alkaloid family is described. This building b...
Progress was made towards the investigation of the stereochemical effects of Ireland-Claisen rearran...
Reaction of Grignard reagents with methyl 3-acetoxy-2-methylenealkanoates produces (2E)-2-substitute...
148 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1987.The product stereoselectivity...
An efficient, stereoselective synthesis of 4′-Ed4T is demonstrated. The synthesis is highlighted by ...
Acid-catalysed thermal rearrangement of 4-aryl-4-methylhex-5-en-2-ones (products of the Claisen rear...
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