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Results 1 - 4 of 4

EC Number	Natural Substrates	Commentary (Nat. Sub.)
3.7.1.18	6-oxocamphor + H2O	-
3.7.1.18	bornane-2,6-dione + H2O	-
3.7.1.18	more	6-oxo camphor hydrolase catalyzes carbon-carbon bond cleavage in bicyclic beta-diketones via a retro-Claisen reaction
3.7.1.18	more	the transformation catalysed by OCH in nature is the cleavage, by a retro-Claisen reaction, of the bicyclic diketone 6-oxocamphor to alpha-campholinic acid, a reaction that proceeds with high diastereoselectivity and enantioselectivity in favour of the (2R,4S)-enantiomer of the product

Results 1 - 4 of 4

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Release 2023.1 (January 2023)