An Unexpected Reaction of Arenesulfonyl Cyanides with Allylic Alcohols: Preparation of Trisubstituted Allyl Sulfones

2008 ◽  
Vol 48 (1) ◽  
pp. 172-174 ◽  
Author(s):  
Leleti Rajender Reddy ◽  
Bin Hu ◽  
Mahavir Prashad ◽  
Kapa Prasad
2008 ◽  
Vol 121 (1) ◽  
pp. 178-180 ◽  
Author(s):  
Leleti Rajender Reddy ◽  
Bin Hu ◽  
Mahavir Prashad ◽  
Kapa Prasad

ChemInform ◽  
2009 ◽  
Vol 40 (19) ◽  
Author(s):  
Leleti Rajender Reddy ◽  
Bin Hu ◽  
Mahavir Prashad ◽  
Kapa Prasad

2012 ◽  
Vol 2 (6) ◽  
pp. 48-48
Author(s):  
Y. M. Nandurkar Y. M. Nandurkar ◽  
◽  
B. B. Bahule B. B. Bahule
Keyword(s):  

2019 ◽  
Author(s):  
Ke-Yin Ye ◽  
Terry McCallum ◽  
Song Lin

Organic radicals are generally short-lived intermediates with exceptionally high reactivity. Strategically, achieving synthetically useful transformations mediated by organic radicals requires both efficient initiation and selective termination events. Here, we report a new catalytic strategy, namely bimetallic radical redox-relay, in the regio- and stereoselective rearrangement of epoxides to allylic alcohols. This approach exploits the rich redox chemistry of Ti and Co complexes and merges reductive epoxide ring opening (initiation) with hydrogen atom transfer (termination). Critically, upon effecting key bond-forming and -breaking events, Ti and Co catalysts undergo proton-transfer/electron-transfer with one another to achieve turnover, thus constituting a truly synergistic dual catalytic system.<br>


2020 ◽  
Vol 59 (46) ◽  
pp. 20394-20398
Author(s):  
Ji Yang ◽  
Jiawang Liu ◽  
Yao Ge ◽  
Weiheng Huang ◽  
Helfried Neumann ◽  
...  

RSC Advances ◽  
2021 ◽  
Vol 11 (28) ◽  
pp. 17025-17031
Author(s):  
Guo-Min Zhang ◽  
Hua Zhang ◽  
Bei Wang ◽  
Ji-Yu Wang
Keyword(s):  

Allylic alcohols can directly dehydrated in water by B(C6F5)3, without any base additives.


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