Abstract: Heteroaryl substituted allyl and homoallyl alcohols were synthesised with two different method. Synthesis of bis-allyl ethers and homoallyl ethers were carried out via reaction of allyl bromide with allyl alcohols and homoallyl alcohols, respectively. [2.3]-Wittig Rearrangement reactions of heteroaryl substituted bis-allyl ethers were investigated using GC/MS techniques. In these reactions two unexpected products were isolated in high yield
Allylation of aldehyde and imine substrates was achieved using easily available allylacetates and di...
Heck-Reactions of homoallyl and allyl alcohols with aromatic dihalogenids give C-C-bond-formation. F...
Allylic alcohol transposition lacks a thermodynamic driving force and usually displays stereo-infide...
Heteroaryl substituted allyl and homoallyl alcohols were synthesised with two different method. Synt...
Substituted homoallylic alcohols have been synthesised both by [2,3]-Wittig rearrangement of unsymme...
Several allyl heteroarylalkyl ethers have been synthesized and then deprotonated with nBuLi in THF a...
Substituted homoallylic alcohols have been synthesised both by [2,3]-Wittig rearrangement of unsymme...
Preceding studies of the butenyl Grignard reagent have indicated a striking tendency on the part of ...
A new and convenient procedure for synthesis of homoallylic alcohols in generally good to excellent ...
Several allyl heteroarylalkyl ethers have been synthesized and then deprotonated with nBuLi in THF a...
The TMS triflate catalyzed allylation of acetals to yield homoallyl ethers proceeds smoothly at room...
A Wittig-Still type [2,3]-sigmatropic rearrangement of (trimethylsilyl)methyl allyl ethers has been ...
In the course of independent investigations in these Laboratories, studies have been made of the pro...
Cleavage of the butenyl Grignard reagent by water gives a mixture of butenes, although the products ...
(I) The solvent and phenyl effects on the rearrangement of hindered homoallylic alkoxides were inves...
Allylation of aldehyde and imine substrates was achieved using easily available allylacetates and di...
Heck-Reactions of homoallyl and allyl alcohols with aromatic dihalogenids give C-C-bond-formation. F...
Allylic alcohol transposition lacks a thermodynamic driving force and usually displays stereo-infide...
Heteroaryl substituted allyl and homoallyl alcohols were synthesised with two different method. Synt...
Substituted homoallylic alcohols have been synthesised both by [2,3]-Wittig rearrangement of unsymme...
Several allyl heteroarylalkyl ethers have been synthesized and then deprotonated with nBuLi in THF a...
Substituted homoallylic alcohols have been synthesised both by [2,3]-Wittig rearrangement of unsymme...
Preceding studies of the butenyl Grignard reagent have indicated a striking tendency on the part of ...
A new and convenient procedure for synthesis of homoallylic alcohols in generally good to excellent ...
Several allyl heteroarylalkyl ethers have been synthesized and then deprotonated with nBuLi in THF a...
The TMS triflate catalyzed allylation of acetals to yield homoallyl ethers proceeds smoothly at room...
A Wittig-Still type [2,3]-sigmatropic rearrangement of (trimethylsilyl)methyl allyl ethers has been ...
In the course of independent investigations in these Laboratories, studies have been made of the pro...
Cleavage of the butenyl Grignard reagent by water gives a mixture of butenes, although the products ...
(I) The solvent and phenyl effects on the rearrangement of hindered homoallylic alkoxides were inves...
Allylation of aldehyde and imine substrates was achieved using easily available allylacetates and di...
Heck-Reactions of homoallyl and allyl alcohols with aromatic dihalogenids give C-C-bond-formation. F...
Allylic alcohol transposition lacks a thermodynamic driving force and usually displays stereo-infide...