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...
Κύριοι συγγραφείς: | Davies, S, Kellie, H, Polywka, R |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
1994
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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ανά: Davies, S, κ.ά.
Έκδοση: (1990) -
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ανά: Davies, S, κ.ά.
Έκδοση: (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
ανά: Cooke, J, κ.ά.
Έκδοση: (1993) -
4-SUBSTITUTED-5,5-DIMETHYL OXAZOLIDIN-2-ONES AS EFFECTIVE CHIRAL AUXILIARIES FOR ENOLATE ALKYLATIONS AND MICHAEL ADDITIONS
ανά: Davies, S, κ.ά.
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