Enzymatic conversion of norsolorinic acid to averufin in aflatoxin biosynthesis

K Yabe1, Y Nakamura, H Nakajima

  • 1National Institute of Animal Health, Ibaraki, Japan.

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Preparation of Amines: Reduction of Oximes and Nitro Compounds

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Preparation of Amines: Reductive Amination of Aldehydes and Ketones

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Preparation of 1° Amines: Hofmann and Curtius Rearrangement Overview

In the presence of an aqueous base and a halogen, primary amides can lose the carbonyl (as carbon dioxide) and undergo rearrangement to form primary amines. This reaction, called the Hofmann rearrangement, can produce primary amines (aryl and alkyl) in high yields without contamination by secondary and tertiary amines.
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2° Amines to N-Nitrosamines: Reaction with NaNO2

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Nitrosation of Enols

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