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Highly Diastereoselective Synthesis of 2-Monosubstituted 1R,5S(1S,5R)-Glycoluriles on the Basis of S- and R-N-Carbamoyl-α-amino Acids.

✍ Scribed by Angelina N. Kravchenko; Konstantin Yu. Chegaev; Il'ya E. Chikunov; Pavel A. Belyakov; Elena Yu. Maksareva; Konstantin A. Lyssenko; Oleg V. Lebedev; Nina N. Makhova


Publisher
John Wiley and Sons
Year
2004
Weight
85 KB
Volume
35
Category
Article
ISSN
0931-7597

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✍ H. TAKIKAWA; K. SHIMBO; K. MORI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Pheromone Synthesis. Part 183. Synthesis of (1R,2R,5S,7R)-and (1R,2S, 5S,7R)-2-Hydroxy-exo-brevicomin, the Components of the Male-Produced Volatiles of the Mountain Pine Beetle, Dendroctonus ponderosae. -Both title compounds (V) and (VI) are synthesized via asymmetric dihydroxylation as the key ste