Journal of Natural Products 2018-03-30

Total Synthesis of (±)-Minfiensine via a Formal [3+2] Cycloaddition

Chao Zhang, Wenzhi Ji, Yahu A. Liu, Chun Song, Xuebin Liao

Index: 10.1021/acs.jnatprod.7b00873

Full Text: HTML

Abstract

(±)-Minfiensine (1) was synthesized in 10 steps in 26% overall yield with the 1,2,3,4-tetrahydro-9a,4a-iminoethanocarbazole core constructed through a [3+2] cycloaddition reaction between indole and an azaoxyallylic cation.

Latest Articles:

Drimane Sesquiterpenoids Noncompetitively Inhibit Human α4β2 Nicotinic Acetylcholine Receptors with Higher Potency Compared to Human α3β4 and α7 Subtypes

2018-04-10

[10.1021/acs.jnatprod.7b00893]

Isolation of Imaqobactin, an Amphiphilic Siderophore from the Arctic Marine Bacterium Variovorax Species RKJM285

2018-04-04

[10.1021/acs.jnatprod.7b00943]

Bioactive α-Pyrone Derivatives from the Endolichenic Fungus Dothideomycetes sp. EL003334

2018-04-04

[10.1021/acs.jnatprod.7b01022]

Total Synthesis of Gramistilbenoids A, B, and C

2018-04-03

[10.1021/acs.jnatprod.7b00865]

Miuramides A and B, Trisoxazole Macrolides from a Mycale sp. Marine Sponge That Induce a Protrusion Phenotype in Cultured Mammalian Cells

2018-04-03

[10.1021/acs.jnatprod.8b00101]

More Articles...