Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Stephan Stanchev"'
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 104:123-133
The addition of α-metallated sulfonamides to cyclic ketones has been studied. Under kinetic control the axial attack of the lithium and the cerium reagents to 4-tert-butylcyclohexanone is preferred, whereas the stereochemical result is inverse when
Publikováno v:
Tetrahedron: Asymmetry. 6:183-198
Synthesis and assignment of the absolute configuration of different types of compounds bearing the diarylmethane moiety is presented. The absolute configuration was determined using chemical correlation and CD approaches based on the sign of the 0-0
Publikováno v:
Tetrahedron: Asymmetry. 4:173-176
Michael addition of methyl vinyl ketone 2 to 2-nitrocycloalkanones 1 catalyzed by the Cinchona alkaloid cinchonine 3 affords adducts in high chemical yields in up to 60% enantiomeric excess. The configuration of the products depends on the ring size.
Publikováno v:
ChemInform. 23
The reaction of racemic 2-phenylpropanal with methyl- and n-butyllithium was studied in detail. Factors such as temperature, solvent, rate of addition, presence of salts, scale-up and source of reagents were carefully examined. Cram-selectivities of
Publikováno v:
ChemInform. 22
A short and efficient synthesis of the title compound based on racemate resolution is described.
Publikováno v:
ChemInform. 22
Publikováno v:
ChemInform. 23
The addition of metallated N,N-dialkyl-sulfonamides 1 to Mannich bases 2, leading to N,N-dialkylamides of 4-(N′,N′-dialkylamino)-2-hydroxy-2-phenylbutanesulfonic acids (4) is described.
Publikováno v:
ChemInform. 24
Transmetalation of organolithium reagents RLi (R = CH3, n-Bu) with manganese pivalate produces reagents of the type RMnOC(O)tBu which react stereoselectively with substituted cyclohexanones to afford the axial alcohols preferentially. These reagents
Publikováno v:
ChemInform. 24
Michael addition of methyl vinyl ketone 2 to 2-nitrocycloalkanones 1 catalyzed by the Cinchona alkaloid cinchonine 3 affords adducts in high chemical yields in up to 60% enantiomeric excess. The configuration of the products depends on the ring size.
Autor:
Manfred T. Reetz, Stephan Stanchev
Publikováno v:
ChemInform. 24
Various organoiron(II) reagents undergo Grignard-type additions to substituted cyclohexanone derivatives, C–C bond formation occurring stereoselectively from the equatorial direction (97–100% selectivity).