Abstract
Chiral N-protected (α-aminoacyl)oxy-substituted terpenes and alkanes, including diastereomeric analogues, are conveniently and efficiently prepared from the corresponding readily available chiral and racemic 1- {[(benzyloxycarbonyl)amino]acyl}benzotriazoles under microwave irradiation with naturally occurring terpene alcohols or alkanols. © Georg Thieme Verlag Stuttgart.
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APA
Katritzky, A. R., & Angrish, P. (2006). Convenient and efficient preparation of N-protected (α-aminoacyl)oxy- substituted terpenes and alkanes. Synthesis, (24), 4135–4142. https://doi.org/10.1055/s-2006-950349
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