The dimerization of Δ1-piperidine-2-carboxylic acid
Keyword(s):
The l-amino acid oxidase of Mytilus edulis has been used to oxidize l-lysine on a large scale in the presence of catalase. The α-oxo acid derived from lysine cyclizes to a Schiff base, which readily dimerizes. The dimer undergoes spontaneous dehydration and decarboxylation to form 1,2,3,4,5,6,7,8-octahydropyrido[3,2-a]-indolizin-10(4bH)-one. This structure was established by a study of its molecular weight and infrared, nuclear-magnetic-resonance and mass spectra.
1970 ◽
Vol 206
(1)
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pp. 181-183
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1982 ◽
Vol 257
(3)
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pp. 1166-1171
1985 ◽
Vol 260
(23)
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pp. 12607-12614
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1968 ◽
Vol 168
(1)
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pp. 156-160
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1961 ◽
Vol 54
(1)
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pp. 199-201
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1968 ◽
Vol 14
(12)
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pp. 1289-1296
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1973 ◽
Vol 327
(2)
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pp. 266-273
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