Synthesis of Marine Alkaloids Isonaamine A, Dorimidazole A, and Preclathridine A. Iminophosphorane-Mediated Preparation of 2-Amino-1,4-disubstituted Imidazoles from α-Azido Esters

1999 ◽  
Vol 64 (7) ◽  
pp. 2540-2544 ◽  
Author(s):  
Pedro Molina ◽  
Pilar M. Fresneda ◽  
Miguel A. Sanz
Keyword(s):  
ChemInform ◽  
2006 ◽  
Vol 37 (37) ◽  
Author(s):  
Pascal Schar ◽  
Sylvaine Cren ◽  
Philippe Renaud

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

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

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):  

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

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

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

Synthesis ◽  
2017 ◽  
Vol 49 (11) ◽  
pp. 2562-2574 ◽  
Author(s):  
Nikita Golantsov ◽  
Alexey Festa ◽  
Alexey Varlamov ◽  
Leonid Voskressensky

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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