Abstract:Organic chemistry honors Icilio Guareschi (1847–1918) with three eponymic reactions, the best known ones being the Guareschi synthesis of pyridones and the Guareschi–Lustgarten reaction. A third Guareschi reaction, the so-called “Guareschi 1897 reaction”, is one of the most unusual reactions in organic chemistry, involving the radical-mediated paradoxical aerobic generation of hydrocarbons in near-neutral water solution. A discussion of the mechanism of this amazing reaction, the only metal-free process that g… Show more
“…61 The scalemate state of asparagine in leguminous seeds was discovered by Arnaldo Piutti in 1886 in vetches ( Vicia sativa L.) seedlings, and his observation of the distinct taste of the two enantiomers of this amino acid was the first report of different physiological effects associated to a pair of enantiomers. 61,62 In the wake of the studies by Guareschi on asparagine, 63 Piutti crystallized 20 kg of the l -enantiomer from an aqueous extract of 6.5 metric tons of germinated vetches, obtaining then a second crop of crystals from the mother liquors. Much to his surprise, the second crystal crop was a conglomerate of hemihedral crystals, from which, by manual (!!)…”
Section: The Origin Of Scalemic Natural Productsmentioning
confidence: 99%
“…Scheme 13 Oxidative coupling of E-coniferyl alcohol (60) to the furofuran lignan pinoresinol ( 61) is followed by stepwise reduction to lariciresinol (62) and to secoisolariciresinol (63). DP = Dirigent protein, PLR = Pinoresinol-lariciresinol reductases.…”
Section: Partial Racemization Of Enantiopure Compoundsmentioning
In natural products, a low optical purity is not generally associated with a sloppy enzymatic activity, but rather with the co-expression of antipodal enzymes/directing proteins or, alternatively, with erosion by enzymatic or spontaneous reactions.
“…61 The scalemate state of asparagine in leguminous seeds was discovered by Arnaldo Piutti in 1886 in vetches ( Vicia sativa L.) seedlings, and his observation of the distinct taste of the two enantiomers of this amino acid was the first report of different physiological effects associated to a pair of enantiomers. 61,62 In the wake of the studies by Guareschi on asparagine, 63 Piutti crystallized 20 kg of the l -enantiomer from an aqueous extract of 6.5 metric tons of germinated vetches, obtaining then a second crop of crystals from the mother liquors. Much to his surprise, the second crystal crop was a conglomerate of hemihedral crystals, from which, by manual (!!)…”
Section: The Origin Of Scalemic Natural Productsmentioning
confidence: 99%
“…Scheme 13 Oxidative coupling of E-coniferyl alcohol (60) to the furofuran lignan pinoresinol ( 61) is followed by stepwise reduction to lariciresinol (62) and to secoisolariciresinol (63). DP = Dirigent protein, PLR = Pinoresinol-lariciresinol reductases.…”
Section: Partial Racemization Of Enantiopure Compoundsmentioning
In natural products, a low optical purity is not generally associated with a sloppy enzymatic activity, but rather with the co-expression of antipodal enzymes/directing proteins or, alternatively, with erosion by enzymatic or spontaneous reactions.
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