Chemo-enzymatic synthesis of bicyclic gamma-lactams using clavaminic acid synthase
Incubation of the γ-lactam analogue of proclavaminic acid, (±)-threo-5-amino-3-hydroxy-2-(1'-aza-2'-oxocyclopentyl) acid, led to production of two bicyclic γ-lactam products.
Κύριοι συγγραφείς: | Baldwin, J, Adlington, R, Bryans, J, Lloyd, MD, Sewell, T, Schofield, C, Baggaley, K, Cassels, R |
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Μορφή: | Journal article |
Έκδοση: |
1997
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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ENZYMATIC-SYNTHESIS OF BICYCLIC GAMMA-LACTAMS USING CLAVAMINIC ACID SYNTHASE
ανά: Baldwin, J, κ.ά.
Έκδοση: (1992) -
SUBSTRATE-ANALOG STUDIES ON CLAVAMINIC ACID SYNTHASE
ανά: Baldwin, J, κ.ά.
Έκδοση: (1993) -
FORMATION OF A NOVEL BICYCLIC GAMMA-LACTAM WITH ISOPENICILLIN-N SYNTHASE
ανά: Baldwin, J, κ.ά.
Έκδοση: (1989) -
STUDIES ON THE STEREOSPECIFICITY OF THE CLAVAMINIC ACID SYNTHASE CATALYZED HYDROXYLATION REACTION
ανά: Baldwin, J, κ.ά.
Έκδοση: (1993) -
Product-substrate engineering by bacteria: Studies on clavaminate synthase, a trifunctional dioxygenase
ανά: Lloyd, MD, κ.ά.
Έκδοση: (1999)