Organic letters

Reactive Intermediates from DMDO Oxidation of Ynamides. Trapping of a de novo Chiral Push-Pull Carbene via Cyclopropanation

ZF Al-Rashid, RP Hsung

Index: Organic Letters, , vol. 10, # 4 p. 661 - 663

Full Text: HTML

Citation Number: 38

Abstract

... Volume: Page: ... Organic Letters. ... by partitioning of the resulting amidoglyoxal 8 9 with its hydrate (confirmed by X-ray), it became clear that (1) ynamide oxidation could be achieved and is relatively faster than reported alkyne oxidations; 10 (2) oxidation of the ...

Related Articles:

Efficient parallel resolution of pentafluorophenyl active esters using quasi-enantiomeric combinations of oxazolidin-2-ones

[Tetrahedron Asymmetry, , vol. 22, # 4 p. 439 - 463]

Efficient parallel resolution of pentafluorophenyl active esters using quasi-enantiomeric combinations of oxazolidin-2-ones

[Tetrahedron Asymmetry, , vol. 22, # 4 p. 439 - 463]

Efficient parallel resolution of pentafluorophenyl active esters using quasi-enantiomeric combinations of oxazolidin-2-ones

[Tetrahedron Asymmetry, , vol. 22, # 4 p. 439 - 463]

Chiral electrophilic “glycinal” equivalents. New synthons for optically active α-amino acids and 4-substituted 2-oxazolidinones

[Matsunaga, Hirofumi; Ishizuka, Tadao; Kunieda, Takehisa Tetrahedron, 1997 , vol. 53, # 4 p. 1275 - 1294]

Highly stereocontrolled synthesis of the 1β-methylcarbapenem key intermediate by the reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives with a …

[Ito; Sasaki; Tamoto; Sunagawa; Terashima Tetrahedron, 1991 , vol. 47, # 16-17 p. 2801 - 2820]

More Articles...