OPENING OF CARBOHYDRATE 5,6-EPOXIDES WITH CHIRAL ACETATE AND PROPIONATE ENOLATE EQUIVALENTS ATTACHED TO THE IRON CHIRAL AUXILIARY [C5H5)FE(CO)(PPH(3))]
The lithium enolate derived from the chiral iron acetyl complex (RS)-[(C5H5)Fe(CO)(PPh3)COCH3] (RS)-1 opens, in the presence of boron trifluoride etherate, the carbohydrate 5,6-epoxides, 5,6-anhydro-3-O-benzyl-1,2-O-isopropylidene-α-D-allofuranose 3, 5,6-anhydro-3-O-benzyl-1,2-O-isopropylidene-β-L-t...
Hlavní autoři: | Davies, S, Kellie, H, Polywka, R |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
1994
|
Podobné jednotky
-
CHIRAL PROPIONATE ENOLATE EQUIVALENT FOR STEREOSELECTIVE ADDITIONS TO SYMMETRICAL KETONES
Autor: Ambler, P, a další
Vydáno: (1985) -
ASYMMETRIC-SYNTHESIS OF 2,4-DISUBSTITUTED BUTYROLACTONES USING THE IRON CHIRAL AUXILIARY [ETA-5-C5H5)FE(CO)(PPH3)]
Autor: Davies, S, a další
Vydáno: (1990) -
CHIRAL ACETATE ENOLATE EQUIVALENT FOR THE SYNTHESIS OF BETA-HYDROXY ACIDS
Autor: Davies, S, a další
Vydáno: (1984) -
STEREOSELECTIVE SYNTHESIS OF (3R,4S)-STATINE UTILIZING THE IRON ACETYL COMPLEX [(ETA-5-C5H5)FE(CO)(PPH3)COME] AS A CHIRAL ACETATE ENOLATE EQUIVALENT
Autor: Cooke, J, a další
Vydáno: (1993) -
4-SUBSTITUTED-5,5-DIMETHYL OXAZOLIDIN-2-ONES AS EFFECTIVE CHIRAL AUXILIARIES FOR ENOLATE ALKYLATIONS AND MICHAEL ADDITIONS
Autor: Davies, S, a další
Vydáno: (1995)