Quaternary Stereocenters:  Challenges and Solutions for Organic Synthesis Edited by Jens Christoffers and Angelika Baro. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany. 2005. xxiii + 336 pp. 17.5 × 24.5 cm. ISBN 3-527-31107-6. $170.00.

2006 ◽  
Vol 49 (8) ◽  
pp. 2666-2666
Author(s):  
Ciro J. Spagnuolo
Science ◽  
2018 ◽  
Vol 361 (6403) ◽  
pp. 664-667 ◽  
Author(s):  
Dainis Kaldre ◽  
Immo Klose ◽  
Nuno Maulide

The chemistry of the carbonyl group is essential to modern organic synthesis. The preparation of substituted, enantioenriched 1,3- or 1,5-dicarbonyls is well developed, as their disconnection naturally follows from the intrinsic polarity of the carbonyl group. By contrast, a general enantioselective access to quaternary stereocenters in acyclic 1,4-dicarbonyl systems remains an unresolved problem, despite the tremendous importance of 2,3-substituted 1,4-dicarbonyl motifs in natural products and drug scaffolds. Here we present a broad enantioselective and stereodivergent strategy to access acyclic, polysubstituted 1,4-dicarbonyls via acid-catalyzed [3,3]-sulfonium rearrangement starting from vinyl sulfoxides and ynamides. The stereochemistry at sulfur governs the absolute sense of chiral induction, whereas the double bond geometry dictates the relative configuration of the final products.


2021 ◽  
Author(s):  
Yong Zhang ◽  
Ya-Kui Sun ◽  
Ya-Ping Chang ◽  
Hui Shao ◽  
Yu-Ming Zhao

Rapid construction of molecules bearing all-substituted quaternary stereocenters represents a highly significant but challenging task in organic synthesis. Herein, we report a novel Palladium-catalyzed cascade between alkene-tethered aryl iodides and...


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