Nature Catalysis, Published online: 16 May 2022; doi:10.1038/s41929-022-00779-2The use of ammonia as a nitrogen source in catalytic asymmetric reactions is attractive but represents a difficult exercise. Now, the asymmetric synthesis of N-unprotected α-amino esters from α-diazoesters and ammonia is achieved by cooperative action of copper complexes and chiral hydrogen-bond donors.
A recent toxicology analysis of the 500-year-old remains of two small children sacrificed in a ritual atop southern Peru’s Ampato volcano showed that the children’s hair and fingernails contained traces of cocaine, as well as two chemical compounds from a flowering vine that’s a key ingredient in the psychedelic beverage ayahuasca.
The compounds in question, harmine and harmaline, are both part of a group of antidepressants called MAOIs (monoamine oxidase inhibitors). The only possible place the Inca could have found these compounds is the flowering vine known to modern science as Banisteriopsis caapi—and to the Indigenous Quechua people as “liana of the dead.” Famously, the liana is one of the two main ingredients in a ritual drink called ayahuasca, which can induce hallucinations or an altered state of mind.
But the analysis found no trace of the compound DMT (N,N-Dimethyltryptamine), which makes ayahuasca such a powerful hallucinogenic. That compound comes from the other main ingredient in ayahuasca, a shrub called chacruna (which, incidentally, is a relative of the plant that gives us coffee).
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