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High‐Yielding Total Synthesis of Sexually Deceptive Chiloglottones and Antimicrobial Dialkylresorcinols through an Organocatalytic Reductive Coupling Reaction
Author(s) -
Madhavachary Rudrakshula,
Ramachary Dhevalapally B.
Publication year - 2014
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201403128
Subject(s) - chemistry , antimicrobial , combinatorial chemistry , coupling (piping) , coupling reaction , organocatalysis , organic chemistry , enantioselective synthesis , catalysis , mechanical engineering , engineering
Biologically important, less‐explored natural products of sexually deceptive chiloglottones, antimicrobial dialkylresorcinols, and their many analogues were synthesized in very good yields in a sequential two‐pot manner by using an “organocatalytic reductive coupling reaction” as the key step.