1986Chemistry LettersRequires access

A NOVEL DECARBOXYLATION OF α-AMINO ACIDS. A FACILE METHOD OF DECARBOXYLATION BY THE USE OF 2-CYCLOHEXEN-1-ONE AS A CATALYST

Mitsunori Hashimoto, Yutaka Eda, Yasutomo Osanai, Toshiaki Iwai, Seiichi Aoki

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Abstract

Abstract In the presence of a catalytic amount of 2-cyclohexen-1-one, decarboxylation of α-amino acids proceeds smoothly and affords the corresponding amino compounds in good yields. Optically active amino compounds, (3R)-(−)-3-hydroxypyrrolidine and (2R)-(−)-2-hydroxypropylamine are obtained in 93% and 80% yields, respectively.

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Abstract In the presence of a catalytic amount of 2-cyclohexen-1-one, decarboxylation of α-amino acids proceeds smoothly and affords the corresponding amino compounds in good yields. Optically active amino compounds, (3R)-(−)-3-hydroxypyrrolidine and (2R)-(−)-2-hydroxypropylamine are obtained in 93% and 80% yields, respectively.

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Available abstract

Abstract In the presence of a catalytic amount of 2-cyclohexen-1-one, decarboxylation of α-amino acids proceeds smoothly and affords the corresponding amino compounds in good yields. Optically active amino compounds, (3R)-(−)-3-hydroxypyrrolidine and (2R)-(−)-2-hydroxypropylamine are obtained in 93% and 80% yields, respectively.

Key concepts: Decarboxylation, Chemistry, Amino acid, Catalysis, Organic chemistry, Biochemistry

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A NOVEL DECARBOXYLATION OF α-AMINO ACIDS. A FACILE METHOD OF DECARBOXYLATION BY THE USE OF 2-CYCLOHEXEN-1-ONE AS A CATALYST — Research Paper | ScholarLens