Synthesis of paraffinic hydrocarbons with two adjacent quaternary carbons

Author(s):  
A. D. Petrov ◽  
L. I. Lavrishcheva
Keyword(s):  
ChemInform ◽  
2012 ◽  
Vol 43 (10) ◽  
pp. no-no
Author(s):  
Yumiko Matsuta ◽  
Takayuki Kobari ◽  
Sachiko Kurashima ◽  
Yuhsuke Kumakura ◽  
Masashi Shinada ◽  
...  

ChemInform ◽  
2005 ◽  
Vol 36 (5) ◽  
Author(s):  
Claude Spino ◽  
Cedrickx Godbout ◽  
Christian Beaulieu ◽  
Magali Harter ◽  
Topwe M. Mwene-Mbeja ◽  
...  

2020 ◽  
Vol 56 (59) ◽  
pp. 8210-8213 ◽  
Author(s):  
Eduardo Palao ◽  
Enol López ◽  
Iván Torres-Moya ◽  
Antonio de la Hoz ◽  
Ángel Díaz-Ortiz ◽  
...  

Formation of all-carbon-substituted quaternary carbons is a key challenge in organic and medicinal chemistry.


Molecules ◽  
2020 ◽  
Vol 25 (17) ◽  
pp. 3841
Author(s):  
Alina Eggert ◽  
Christoph Etling ◽  
Dennis Lübken ◽  
Marius Saxarra ◽  
Markus Kalesse

Contiguous quaternary carbons in terpene natural products remain a major challenge in total synthesis. Synthetic strategies to overcome this challenge will be a pivotal prerequisite to the medicinal application of natural products and their analogs or derivatives. In this review, we cover syntheses of natural products that exhibit a dense assembly of quaternary carbons and whose syntheses were uncompleted until recently. While discussing their syntheses, we not only cover the most recent total syntheses but also provide an update on the status quo of modern syntheses of complex natural products. Herein, we review (±)-canataxpropellane, (+)-waihoensene, (–)-illisimonin A and (±)-11-O-debenzoyltashironin as prominent examples of natural products bearing contiguous quaternary carbons.


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