Catalysis-based enantioselective total synthesis of the macrocyclic spermidine alkaloid isooncinotine.
about
Formal ring-opening/cross-coupling reactions of 2-pyrones: iron-catalyzed entry into stereodefined dienyl carboxylates.Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partnersIron-catalyzed alkylations of aryl sulfamates and carbamates.Iron-catalysed cross-coupling of organolithium compounds with organic halides.Iron-promoted C-C bond formation in the total synthesis of natural products and drugs.Iron-Catalyzed C-C Cross-Couplings Using Organometallics.Catalytic Dearomatization of N-Heteroarenes with Silicon and Boron Compounds.Molecular editing and assessment of the cytotoxic properties of iejimalide and progeny.Gram-scale synthesis of iejimalide B.Total synthesis of nominal gobienine A.Total syntheses of the actin-binding macrolides latrunculin A, B, C, M, S and 16-epi-latrunculin B.
P2860
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P2860
Catalysis-based enantioselective total synthesis of the macrocyclic spermidine alkaloid isooncinotine.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 12 May 2004
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Catalysis-based enantioselecti ...... midine alkaloid isooncinotine.
@en
Catalysis-based enantioselecti ...... midine alkaloid isooncinotine.
@nl
type
label
Catalysis-based enantioselecti ...... midine alkaloid isooncinotine.
@en
Catalysis-based enantioselecti ...... midine alkaloid isooncinotine.
@nl
prefLabel
Catalysis-based enantioselecti ...... midine alkaloid isooncinotine.
@en
Catalysis-based enantioselecti ...... midine alkaloid isooncinotine.
@nl
P2860
P356
P1476
Catalysis-based enantioselecti ...... midine alkaloid isooncinotine.
@en
P2093
Andreas Leitner
Bodo Scheiper
P2860
P304
11960-11965
P356
10.1073/PNAS.0401322101
P407
P577
2004-05-12T00:00:00Z