ChemInform Abstract: A NEW TYPE OF PHOSPHORUS-CARBON AND CARBON-CARBON BOND CLEAVAGE REACTIONS IN α-(TRIMETHYLSILYLOXY)-β-OXO PHOSPHONATES AND α-ETHOXY-β-OXO PHOSPHONATES. THE SYNTHESIS OF UNSYMMETRICAL α-HYDROXY KETONES UTILIZING 1:1 CARBONYL ADDUCTS OF

1982 ◽  
Vol 13 (17) ◽  
Author(s):  
M. SEKINE ◽  
H. NAKAJIMA ◽  
T. HATA
2019 ◽  
Vol 48 (9) ◽  
pp. 2615-2656 ◽  
Author(s):  
Paramasivam Sivaguru ◽  
Zikun Wang ◽  
Giuseppe Zanoni ◽  
Xihe Bi

This review provides insights into the in situ generated radicals triggered carbon–carbon bond cleavage reactions.


2016 ◽  
Vol 55 (14) ◽  
pp. 6916-6928 ◽  
Author(s):  
Sushma L. Saraf ◽  
Anna Miłaczewska ◽  
Tomasz Borowski ◽  
Christopher D. James ◽  
David L. Tierney ◽  
...  

1982 ◽  
Vol 11 (10) ◽  
pp. 1607-1610 ◽  
Author(s):  
Masanori Utaka ◽  
Yuji Fujita ◽  
Akira Takeda

Author(s):  
Yong Zhang ◽  
Guo-Wei Lai ◽  
Long-Jun Nie ◽  
Qifang He ◽  
Mei-Juan Lin ◽  
...  

α-aryl-α,α-Difluoroacetophenones (DFAPs) are developed as a new type of difluorobenzylation reagents that can be facilely prepared from readily available and cheap starting materials. In-situ carbon-carbon bond cleavage of electron-deficient DFAPs...


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