scholarly journals Facile Amberlyst A-21 catalyzed access of β-hydroxynitriles via epoxide opening in water

2020 ◽  
Vol 13 (11) ◽  
pp. 8200-8208
Author(s):  
M. Shaheer Malik ◽  
Basim H. Asghar ◽  
Shaik Azeeza ◽  
Rami J. Obaid ◽  
Ismail I. Thagafi ◽  
...  
Keyword(s):  
2020 ◽  
Vol 59 (42) ◽  
pp. 18473-18478
Author(s):  
Feng‐Xing Li ◽  
Shu‐Jian Ren ◽  
Pei‐Fang Li ◽  
Peng Yang ◽  
Jin Qu

Synlett ◽  
2021 ◽  
Author(s):  
Stefan Schulz ◽  
Dennis Poth ◽  
Pardha Saradhi Peram ◽  
Susann Hötling ◽  
Markus Menke ◽  
...  

AbstractFor a long time, frogs were believed to communicate primarily via the acoustic channel, but during the last decades it became obvious that various lineages also use chemical communication. In this Account we present our research on the identification of volatile lactones from Madagascan Mantellidae and African Hyperoliidae frogs. Both possess male specific glands that can disseminate a range of volatile compounds. Key constituents are macrocyclic lactones. They show high variability in structure and occurrence. We focus here on the synthetic approaches we have used to clarify constitution and configuration of the glandular compounds. Key synthetic methods are ring-closing metathesis and nucleophilic epoxide opening. Often, but not always, the natural compounds occurs in amounts that excludes their investigation by NMR spectroscopy. Instead, we use GC/MS analysis, GC/IR, microreactions, and synthesis to identify such components. Several aspects of our work will be described giving some insight in our scientific approach.1 Introduction2 Macrocylic Lactones from the Fatty Acid Biosynthetic Pathway3 Unsaturated Lactones4 Terpenoid Lactones5 Macrolide Occurrence6 Conclusions


1991 ◽  
Vol 32 (5) ◽  
pp. 611-614 ◽  
Author(s):  
Harald Baumgartner ◽  
Christoph Marschner ◽  
Rainer Pucher ◽  
Herfried Griengl

1981 ◽  
Vol 59 (10) ◽  
pp. 1415-1424 ◽  
Author(s):  
John M. Decesare ◽  
Bernard Corbel ◽  
Tony Durst ◽  
John F. Blount

γ-Epoxy sulfones in which the epoxide function is terminal yield cyclopropylmethanol derivatives on reaction with methyllithium or lithium diisopropylamide. In contrast, treatment of these epoxides with two equivalents of CH3MgI gives only cis-3-phenylsulfonylcyclobutanols. The cis-relationship between the OH and sulfonyl groups was proven in one instance by an X-ray structure determination. Internal γ-epoxy sulfones yield cyclopropylmethanols with all bases studied. All δ-epoxy sulfones studied furnished cis-3-phenylsulfonylcyclopentanols upon reaction with the Grignard reagent. These same epoxides gave either cyclopentanols or noncyclic products upon reaction with LDA; no cyclobutane ring containing products were obtained contrary to the expectations based on Stork's results with the corresponding epoxy nitriles (ref. 2). The mechanism of the Grignard-mediated reaction involves epoxide opening by iodide ion, α-sulfonyl Grignard formation, and, finally, cyclization. When LDA or CH3Li is used the products are formed by an intramolecular SN2 opening of the epoxide by an α-lithio sulfone.


2007 ◽  
Vol 129 (5) ◽  
pp. 1359-1371 ◽  
Author(s):  
Andreas Gansäuer ◽  
Andriy Barchuk ◽  
Florian Keller ◽  
Martin Schmitt ◽  
Stefan Grimme ◽  
...  

ChemInform ◽  
2009 ◽  
Vol 40 (40) ◽  
Author(s):  
Christopher J. Morten ◽  
Timothy F. Jamison
Keyword(s):  

2011 ◽  
Vol 21 (8) ◽  
pp. 2510-2514 ◽  
Author(s):  
Aline Banchet-Cadeddu ◽  
Agathe Martinez ◽  
Stéphane Guillarme ◽  
Véronique Parietti ◽  
Fanny Monneaux ◽  
...  

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