Stereoselectivity of formation of monoterpene – Amino acids hybrid molecules in the reaction of monoterpene nitroso chlorides with α-amino acid derivatives

Reaction of nitrosochlorides of natural monoterpene hydrocarbons (+)-3-carene and (−)-α-pinene with L-amino acids and their methyl esters results in stereoselective formation of terpene–amino acids hybrids, which belong to the series of α-substituted amino oximes. The reaction with an excess of race...

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Veröffentlicht in:	Steroids 2017-01, Vol.117, p.112-119
Hauptverfasser:	Marenin, K.S., Gatilov, Yu.V., Agafontsev, A.M., Tkachev, A.V.
Format:	Artikel
Sprache:	eng
Schlagworte:	(+)-3-Carene (−)-α-Pinene Amino acids Amino Acids - chemistry Diastereoselectivity Magnetic Resonance Spectroscopy Monoterpenes - chemistry Nitroso chlorides Stereoisomerism Terpenes - chemistry
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