Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Elaine Lebeau"'
Publikováno v:
The Journal of Organic Chemistry. 59:4868-4874
A novel and efficient method for the oxidative glycosidation at the heterosubstituted benzylic positions with 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) is described. The reaction is stereospecific with 3-substituted isochromans and isothiochroman, a
Publikováno v:
Tetrahedron Letters. 35:6207-6210
The use of magnesium metal in methanol for the deprotection of alkyl esters is described. This mild reagent also provides good to excellent selectivity to cleave different esters. The order of the reactivity of this reagent towards acyl cleavages was
Publikováno v:
Tetrahedron Letters. 34:8189-8192
2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) induced functionalization at the heterosubstituted benzylic position with a variety of carbon nucleophiles proceeds in high yield with good stereochemical control.
Publikováno v:
Tetrahedron Letters. 34:3841-3844
2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) induced oxidative coupling of isochromans or isothiochroman and alcohols proceeds in high yield with good regio- and stereochemical control.
Publikováno v:
ChemInform. 24
2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) induced oxidative coupling of isochromans or isothiochroman and alcohols proceeds in high yield with good regio- and stereochemical control.
Publikováno v:
ChemInform. 25
3-Carbonyl substituted isothiochromans (3,4-dihydro-1H-2-benzothio- pyrans) (3) were synthesized in moderate yields in a one-pot process from dibromide (1) and 2-mercaptocarbonyl compounds (2). This method could be also extended to the synthesis of t
Publikováno v:
ChemInform. 26
A novel and efficient method for the oxidative glycosidation at the heterosubstituted benzylic positions with 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) is described. The reaction is stereospecific with 3-substituted isochromans and isothiochroman, a
Publikováno v:
ChemInform. 26
The use of magnesium metal in methanol for the deprotection of alkyl esters is described. This mild reagent also provides good to excellent selectivity to cleave different esters. The order of the reactivity of this reagent towards acyl cleavages was
Publikováno v:
Synthesis. 1994:363-365
3-Carbonyl substituted isothiochromans (3,4-dihydro-1H-2-benzothio- pyrans) (3) were synthesized in moderate yields in a one-pot process from dibromide (1) and 2-mercaptocarbonyl compounds (2). This method could be also extended to the synthesis of t