ChemInform Abstract: Synthesis of the Brominated Marine Alkaloids (.+-.)-Arborescidine A (IV), B (VIII), and C (VI).

ChemInform ◽  
2010 ◽  
Vol 29 (35) ◽  
pp. no-no
Author(s):  
B. E. A. BURM ◽  
M. M. MEIJLER ◽  
J. KORVER ◽  
M. J. WANNER ◽  
G.-J. KOOMEN
Keyword(s):  
Marine Alkaloids

Tricyclic Marine Alkaloids: Synthetic Approaches to Cylindricines, Lepadiformine, and Fasicularin

ChemInform ◽  
2006 ◽  
Vol 37 (37) ◽  
Author(s):  
Pascal Schar ◽  
Sylvaine Cren ◽  
Philippe Renaud
Keyword(s):  
Marine Alkaloids ◽  
Synthetic Approaches

ChemInform Abstract: The First Synthesis of the Pentacyclic Pyridoacridine Marine Alkaloids: Arnoamines A (XII) and B (XI).

ChemInform ◽  
2000 ◽  
Vol 31 (51) ◽  
pp. no-no
Author(s):  
Evelyne Delfourne ◽  
Celine Roubin ◽  
Jean Bastide
Keyword(s):  
Marine Alkaloids

scholarly journals Marine Alkaloids. 11. Flustramide B and Flustrarine B from the Marine Bryozoan Flustra foliacea. Synthesis of Flustrarine B.

1986 ◽  
Vol 40b ◽  
pp. 555-558 ◽  
Author(s):  
Pernille Keil ◽  
Elisabeth G. Nielsen ◽  
Uffe Anthoni ◽  
Carsten Christophersen ◽  
Povl Krogsgaard-Larsen ◽  
...  
Keyword(s):  
Marine Alkaloids ◽  
Marine Bryozoan ◽  
Flustra Foliacea

Short and Flexible Route to 3,4-Diarylpyrrole Marine Alkaloids: Syntheses of Permethyl Storniamide A (I), Ningalin B (II), and Lamellarin G Trimethyl Ether (III).

ChemInform ◽  
2003 ◽  
Vol 34 (38) ◽  
Author(s):  
Masatomo Iwao ◽  
Toshiro Takeuchi ◽  
Naotaka Fujikawa ◽  
Tsutomu Fukuda ◽  
Fumito Ishibashi
Keyword(s):  
Marine Alkaloids ◽  
Trimethyl Ether

ChemInform Abstract: Synthetic Approaches to the Eudistomin Marine Alkaloids

ChemInform ◽  
2010 ◽  
Vol 31 (34) ◽  
pp. no-no
Author(s):  
J. McNulty ◽  
I. W. J. Still
Keyword(s):  
Marine Alkaloids ◽  
Synthetic Approaches

Tryptophan derived natural marine alkaloids and synthetic derivatives as promising antimicrobial agents

2021 ◽  
Vol 209 ◽  
pp. 112945
Author(s):  
Mariana C. Almeida ◽  
Diana I.S.P. Resende ◽  
Paulo M. da Costa ◽  
Madalena M.M. Pinto ◽  
Emília Sousa
Keyword(s):  
Antimicrobial Agents ◽  
Marine Alkaloids ◽  
Synthetic Derivatives

scholarly journals Revision of the Structure and Total Synthesis of Topsentin C

Synthesis ◽  
2017 ◽  
Vol 49 (11) ◽  
pp. 2562-2574 ◽  
Author(s):  
Nikita Golantsov ◽  
Alexey Festa ◽  
Alexey Varlamov ◽  
Leonid Voskressensky
Keyword(s):  
Total Synthesis ◽  
Secondary Metabolite ◽  
Conjugate Addition ◽  
Solvent Free ◽  
Synthetic Approach ◽  
Protecting Group ◽  
Marine Alkaloids ◽  
Mild Reduction

An efficient synthetic approach to access (indol-3-yl)ethane-1,2-diamines with a protecting group at the indole N atom from readily available 3-(2-nitrovinyl)indoles is reported. This approach includes solvent-free conjugate addition of O-pivaloylhydroxylamines to 1-Boc-3-(2-nitrovinyl)indoles followed by mild reduction of the adducts. The obtained (indol-3-yl)ethane-1,2-diamines are convenient synthetic precursors for several classes of marine alkaloids. The first total synthesis of racemic topsentin C, a secondary metabolite from Hexadella sp., based on this approach is reported. The initially proposed structure for topsentin C has been revised.

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