Cu-mediated enamide formation in the total synthesis of complex peptide natural products.
about
Application of the aza-Diels-Alder reaction in the synthesis of natural products.The total synthesis and functional evaluation of fourteen stereoisomers of yaku'amide B. The importance of stereochemistry for hydrophobicity and cytotoxicity.Studies on the synthesis of peptides containing dehydrovaline and dehydroisoleucine based on copper-mediated enamide formation.Isomerization of N-Allyl Amides To Form Geometrically Defined Di-, Tri-, and Tetrasubstituted Enamides.Oxidative couplings on tryptophan-based diketopiperazines leading to fused and bridged chemotypes.Total synthesis of the reported structure of ceanothine D via a novel macrocyclization strategy.
P2860
Cu-mediated enamide formation in the total synthesis of complex peptide natural products.
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artigo científico
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Cu-mediated enamide formation in the total synthesis of complex peptide natural products.
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Cu-mediated enamide formation in the total synthesis of complex peptide natural products.
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prefLabel
Cu-mediated enamide formation in the total synthesis of complex peptide natural products.
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P2093
P2860
P356
P1476
Cu-mediated enamide formation in the total synthesis of complex peptide natural products.
@en
P2093
Masayuki Inoue
Takefumi Kuranaga
Yusuke Sesoko
P2860
P304
P356
10.1039/C3NP70103D
P577
2014-02-25T00:00:00Z