Complexity generation by chemical synthesis: a five-step synthesis of (-)-chaetominine from L-tryptophan and its biosynthetic implications.
about
Recent developments in the chemistry of quinazolinone alkaloids.Rhodium-Catalyzed Asymmetric N-H Functionalization of Quinazolinones with Allenes and Allylic Carbonates: The First Enantioselective Formal Total Synthesis of (-)-Chaetominine.Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline.Efficient oxidation of N-protected tryptophan and tryptophanyl-dipeptides by in situ generated dimethyldioxirane provides hexahydropyrroloindoline-containing synthons suitable for peptide synthesis and subsequent tryptathionylation.
P2860
Complexity generation by chemical synthesis: a five-step synthesis of (-)-chaetominine from L-tryptophan and its biosynthetic implications.
description
2014 nî lūn-bûn
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name
Complexity generation by chemi ...... its biosynthetic implications.
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Complexity generation by chemical synthesis: a five-step synthesis of
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type
label
Complexity generation by chemi ...... its biosynthetic implications.
@en
Complexity generation by chemical synthesis: a five-step synthesis of
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prefLabel
Complexity generation by chemi ...... its biosynthetic implications.
@en
Complexity generation by chemical synthesis: a five-step synthesis of
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P2093
P2860
P356
P1476
Complexity generation by chemi ...... its biosynthetic implications.
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P2093
Chu-Pei Xu
Shi-Peng Luo
P2860
P304
P356
10.1039/C4OB00314D
P577
2014-05-01T00:00:00Z