| 1. | Metabolism involves first oxidation by monoamine oxidase to the corresponding aldehyde.
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| 2. | For instance cinnamaldehyde presents both aliphatic double bond and aldehyde function.
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| 3. | The biosynthesis of atropine starting from P450 enzyme forming hyoscyamine aldehyde.
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| 4. | Dicarbonyls react with amine to produce Strecker aldehyde through Strecker degradation.
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| 5. | These enzymes are members of the larger class of aldehyde dehydrogenases.
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| 6. | Sodium borohydride reduces aldehydes and ketones to give the related alcohols.
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| 7. | Glutamic acid was converted to the necessary aldehyde via Strecker degradation.
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| 8. | A cysteine and a glutamate will interact with the aldehyde substrate.
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| 9. | Possible reactivity at aldehydes include nucleophilic attack and addition of allylmetals.
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| 10. | Aldehydes with no ?-hydrogens can undergo the Tishchenko reaction.
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