cyclic alkenes
Recently Published Documents


TOTAL DOCUMENTS

161
(FIVE YEARS 17)

H-INDEX

26
(FIVE YEARS 3)

Author(s):  
Damon J. Gilmour ◽  
Tanja Tomkovic ◽  
Nirmalendu Kuanr ◽  
Mitchell R. Perry ◽  
Hans Gildenast ◽  
...  

2021 ◽  
Author(s):  
Alex J. Vendola ◽  
Christophe Allais ◽  
Anne-Marie R. Dechert-Schmitt ◽  
James T. Lee ◽  
Robert A. Singer ◽  
...  
Keyword(s):  

Author(s):  
Roman S. Ishigeev ◽  
Vladimir A. Potapov ◽  
Irina V. Skurchenko ◽  
Alfiya G. Khabibulina ◽  
Svetlana V. Amosova

2021 ◽  
Author(s):  
Zehao Yu ◽  
Zinan Dai ◽  
Ying Bai ◽  
Jiayun Li ◽  
Yan Yan ◽  
...  

A convenient metal-free photocatalytic hydrosilylation of variety of linear and cyclic alkenes have been investigated. It was found that the free radical type photoinitiator Irgacure 2959 had a better effect...


Author(s):  
Samuel Charles Brydon ◽  
Gabriel da Silva ◽  
Richard OHair ◽  
Jonathan White

Haliranium ions are intermediates often involved in complex cyclisations, where their structure allows for control over stereospecific outcomes. Extending previous studies into their structure and reactivity in the gas phase,...


Synthesis ◽  
2020 ◽  
Author(s):  
Yasuyuki Ura

AbstractCatalytic anti-Markovnikov (AM) oxidation of terminal alkenes can provide terminally oxyfunctionalized organic compounds. This short review mainly summarizes our recent progress on the Pd-catalyzed AM oxidations of aromatic and aliphatic terminal alkenes to give terminal acetals (oxidative acetalization) and aldehydes (Wacker-type oxidation), along with related reports. These reactions demonstrate the efficacy of the PdCl2(MeCN)2/CuCl/electron-deficient cyclic alkenes/O2 catalytic system. Notably, electron-deficient cyclic alkenes such as p-benzoquinones (BQs) and maleimides are key additives that facilitate nucleophilic attack of oxygen nucleophiles on coordinated terminal alkenes and enhance the AM selectivity. BQs also function to oxidize Pd(0) depending on the reaction conditions. Several other factors that improve the AM selectivity, such as the steric demand of the nucleo­philes, slow substrate addition, and halogen-directing groups, are also discussed.1 Introduction2 Anti-Markovnikov Oxidation of Aromatic Alkenes to Terminal Acetals­3 Anti-Markovnikov Oxidation of Aromatic Alkenes to Aldehydes4 Anti-Markovnikov Oxidation of Aliphatic Alkenes to Terminal Acetals­5 Anti-Markovnikov Oxidation of Aliphatic Alkenes to Aldehydes6 Conclusion


2020 ◽  
Vol 85 (21) ◽  
pp. 13557-13566
Author(s):  
Jorge Escorihuela ◽  
Wilhelmus J. E. Looijen ◽  
Xiao Wang ◽  
Adelia J. A. Aquino ◽  
Hans Lischka ◽  
...  

2020 ◽  
Vol 142 (43) ◽  
pp. 18330-18335
Author(s):  
Oliver P. E. Townrow ◽  
Cheuk Chung ◽  
Stuart A. Macgregor ◽  
Andrew S. Weller ◽  
Jose M. Goicoechea

Sign in / Sign up

Export Citation Format

Share Document