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Predominately Uncultured Microbes as Sources of Bioactive AgentsMetabolite localization by atmospheric pressure high-resolution scanning microprobe matrix-assisted laser desorption/ionization mass spectrometry imaging in whole-body sections and individual organs of the rove beetle Paederus riparius.Temporary restraints to overcome steric obstacles: an efficient strategy for the synthesis of mycalamide B.Total synthesis and isolation of citrinalin and cyclopiamine congeners.Total synthesis of pederin and analoguesMulticomponent approach to the synthesis of oxidized amides through nitrile hydrozirconationTotal synthesis of irciniastatin A (Psymberin).Isolation, biological activity, synthesis, and medicinal chemistry of the pederin/mycalamide family of natural products.Strategies for the construction of tetrahydropyran rings in the synthesis of natural products.The protein synthesis inhibitors mycalamides A and E have limited susceptibility toward the drug efflux network.Organocatalytic regioselective asymmetric Michael addition of azlactones to o-hydroxy chalcone derivatives.
P2860
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P2860
description
article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2007
@uk
name
Total Synthesis of Pederin
@en
Total Synthesis of Pederin
@nl
type
label
Total Synthesis of Pederin
@en
Total Synthesis of Pederin
@nl
prefLabel
Total Synthesis of Pederin
@en
Total Synthesis of Pederin
@nl
P921
P356
P1476
Total Synthesis of Pederin
@en
P2093
John C. Jewett
Viresh H. Rawal
P304
P356
10.1002/ANIE.200701677
P407
P577
2007-08-27T00:00:00Z