The intramolecular [2 + 2] cycloaddition of keteniminium salt 5 derived from (2S, 5S)-dimethylpyrrolidine is the key step of a short synthetic route toward prostaglandins
SIGLEAvailable from British Library Document Supply Centre- DSC:D40138/82 / BLDSC - British Library ...
Synthesis of nitrogenated quaternary centered polyhydroxylated aminocyclopentanes by implementation ...
Acetoxyfulvene surrended to asymmetric Diels␣ Alder cycloaddition, paving the way to the development...
lecular [2+2] cycloaddition of an α,β-unsaturated keteniminium salt is the key step of a short synth...
Intramolecular [2 + 2] Cyclo-additions of Ketenes and Keteniminium Salts To Olefin
An efficient and stereocontrolled synthesis of prostaglandins from cyclopentadiene monoepoxide is de...
The objective of this study was to explore intramolecular ketene cycloadditions with the anticipated...
The many potent biological affects of the prostaglandins make this family of compounds and their str...
The compatibility of nitromethane conjugate addition to 2-cyclo-pentenones bearing a 4-oxygenated fu...
Prostaglandins are an important class of biologically active compounds. The robust syntheses of diff...
The stereoselective intramolecular cyclizations of bis(cinnamyl)tosylamides and dimethyl bis(cinnamy...
Five-membered rings are ubiquitous in natural and biologically relevant products. Among the plethora...
The synthesis of an important intermediate (36) in a total synthesis of the prostaglandins was under...
Efficient lithium amide-induced intramolecular cyclopropanation of bishomoallylic and trishomoallyli...
A novel total synthesis of (dl)-prostaglandin F1α methyl ester is described. The 2,3-dialkyl-1,4-cyc...
SIGLEAvailable from British Library Document Supply Centre- DSC:D40138/82 / BLDSC - British Library ...
Synthesis of nitrogenated quaternary centered polyhydroxylated aminocyclopentanes by implementation ...
Acetoxyfulvene surrended to asymmetric Diels␣ Alder cycloaddition, paving the way to the development...
lecular [2+2] cycloaddition of an α,β-unsaturated keteniminium salt is the key step of a short synth...
Intramolecular [2 + 2] Cyclo-additions of Ketenes and Keteniminium Salts To Olefin
An efficient and stereocontrolled synthesis of prostaglandins from cyclopentadiene monoepoxide is de...
The objective of this study was to explore intramolecular ketene cycloadditions with the anticipated...
The many potent biological affects of the prostaglandins make this family of compounds and their str...
The compatibility of nitromethane conjugate addition to 2-cyclo-pentenones bearing a 4-oxygenated fu...
Prostaglandins are an important class of biologically active compounds. The robust syntheses of diff...
The stereoselective intramolecular cyclizations of bis(cinnamyl)tosylamides and dimethyl bis(cinnamy...
Five-membered rings are ubiquitous in natural and biologically relevant products. Among the plethora...
The synthesis of an important intermediate (36) in a total synthesis of the prostaglandins was under...
Efficient lithium amide-induced intramolecular cyclopropanation of bishomoallylic and trishomoallyli...
A novel total synthesis of (dl)-prostaglandin F1α methyl ester is described. The 2,3-dialkyl-1,4-cyc...
SIGLEAvailable from British Library Document Supply Centre- DSC:D40138/82 / BLDSC - British Library ...
Synthesis of nitrogenated quaternary centered polyhydroxylated aminocyclopentanes by implementation ...
Acetoxyfulvene surrended to asymmetric Diels␣ Alder cycloaddition, paving the way to the development...
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