The cascade radical cyclisation approach to prenylated alkaloids: synthesis of stephacidin A and notoamide B.
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Intermolecular Diels-Alder Cycloaddition for the Construction of Bicyclo[2.2.2]diazaoctane Structures: Formal Synthesis of Brevianamide B and PremalbrancheamideUnified Approach to Prenylated Indole Alkaloids: Total Syntheses of (-)-17-Hydroxy-Citrinalin B, (+)-Stephacidin A, and (+)-Notoamide I.Bioinspired chemical synthesis of monomeric and dimeric stephacidin A congeners.Total Synthesis of Notoamides F, I, and R and Sclerotiamide.Evidence of single electron transfer from the enolate anion of an N,N'-dialkyldiketopiperazine additive in BHAS coupling reactions.Total synthesis of (-)-depyranoversicolamide B.Simple indole alkaloids and those with a nonrearranged monoterpenoid unitStructural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi
P2860
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P2860
The cascade radical cyclisation approach to prenylated alkaloids: synthesis of stephacidin A and notoamide B.
description
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name
The cascade radical cyclisatio ...... stephacidin A and notoamide B.
@en
The cascade radical cyclisatio ...... stephacidin A and notoamide B.
@nl
type
label
The cascade radical cyclisatio ...... stephacidin A and notoamide B.
@en
The cascade radical cyclisatio ...... stephacidin A and notoamide B.
@nl
prefLabel
The cascade radical cyclisatio ...... stephacidin A and notoamide B.
@en
The cascade radical cyclisatio ...... stephacidin A and notoamide B.
@nl
P2093
P2860
P356
P1476
The cascade radical cyclisatio ...... stephacidin A and notoamide B.
@en
P2093
Ilias Pavlakos
Louise Male
Michael D Weller
Nigel S Simpkins
P2860
P304
P356
10.1039/C3OB40979A
P577
2013-06-25T00:00:00Z