Stereoselective Synthesis of C5−C20 and C21−C34 Subunits of the Core Structure of the Aplyronines. Applications of Enantioselective Additions of Chiral Allenylindium Reagents to Chiral Aldehydes

2000 ◽  
Vol 65 (5) ◽  
pp. 1501-1510 ◽  
Author(s):  
James A. Marshall ◽  
Brian A. Johns
Keyword(s):  
Stereoselective Synthesis ◽  
Core Structure ◽  
The Core

Stereoselective synthesis of an eleganine A core

2020 ◽  
Vol 18 (24) ◽  
pp. 4566-4568
Author(s):  
Gints Smits ◽  
Ronalds Zemribo
Keyword(s):  
Stereoselective Synthesis ◽  
Core Structure ◽  
The Core ◽  
First Time

The core structure of eleganine A – a cytotoxic indole monoterpene alkaloid – was accessed for the first time.

ChemInform Abstract: Stereoselective Synthesis of the Core Structure of the Nephritogenoside Glycopeptide.

ChemInform ◽  
2010 ◽  
Vol 28 (50) ◽  
pp. no-no
Author(s):  
H. ZHANG ◽  
Y. WANG ◽  
R. THUERMER ◽  
M. MEISENBACH ◽  
W. VOELTER
Keyword(s):  
Stereoselective Synthesis ◽  
Core Structure ◽  
The Core

Stereoselective Synthesis of the Core Structure of the Nephritogenoside Glycopeptide

1997 ◽  
Vol 1997 (9) ◽  
pp. 1871-1876 ◽  
Author(s):  
Hong Zhang ◽  
Yali Wang ◽  
René Thürmer ◽  
Mark Meisenbach ◽  
Wolfgang Voelter
Keyword(s):  
Stereoselective Synthesis ◽  
Core Structure ◽  
The Core

Stereoselective synthesis of 3-amino-2-oxindoles from isatin imines: new scaffolds for bioactivity evaluation

RSC Advances ◽  
2015 ◽  
Vol 5 (65) ◽  
pp. 52481-52496 ◽  
Author(s):  
Jasneet Kaur ◽  
Swapandeep Singh Chimni ◽  
Suhel Mahajan ◽  
Akshay Kumar
Keyword(s):  
Natural Products ◽  
Stereoselective Synthesis ◽  
Core Structure ◽  
Drug Candidates ◽  
The Core

3-Substituted-3-aminooxindole motifs constitute the core structure of a number of natural products and drug candidates.

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