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Cover Feature: Enantioselective Synthesis of a Tricyclic, sp 3 ‐Rich Diazatetradecanedione: an Amino Acid‐Based Natural Product‐Like Scaffold (Chem. Eur. J. 21/2020)
Author(s) -
Bischoff Matthias,
Mayer Peter,
Meyners Christian,
Hausch Felix
Publication year - 2020
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202000858
Subject(s) - enantioselective synthesis , tricyclic , natural product , cover (algebra) , scaffold , chemistry , combinatorial chemistry , stereochemistry , amino acid , feature (linguistics) , organic chemistry , computer science , catalysis , biochemistry , engineering , programming language , mechanical engineering , linguistics , philosophy
Fishing in the chiral pool , while envisaging sp 3 ‐rich molecules. Using simple amino acids as starting materials, a synthetic method was designed to construct a rigid, tricyclic sp 3 ‐rich scaffold consisting of six‐, seven‐, and eight‐membered rings. More information can be found in the Communication by M. Bischoff, F. Hausch et al. on page 4677.