ChemInform Abstract: Et3B-Induced Stereoselective Radical Addition of Ph3GeH to Carbon-Carbon Multiple Bonds and Its Application to Isomerization of Olefins.

ChemInform ◽  
1990 ◽  
Vol 21 (49) ◽  
Author(s):  
K. NOZAKI ◽  
Y. ICHINOSE ◽  
K. WAKAMATSU ◽  
K. OSHIMA ◽  
K. UTIMOTO
1990 ◽  
Vol 63 (8) ◽  
pp. 2268-2272 ◽  
Author(s):  
Kyoko Nozaki ◽  
Yoshifumi Ichinose ◽  
Kuni Wakamatsu ◽  
Koichiro Oshima ◽  
Kiitiro Utimoto

2020 ◽  
Vol 16 ◽  
pp. 502-508
Author(s):  
Goki Hirata ◽  
Yu Yamane ◽  
Naoya Tsubaki ◽  
Reina Hara ◽  
Takashi Nishikata

A terminal alkyne is one of the most useful reactants for the synthesis of alkyne and alkene derivatives. Because an alkyne undergoes addition reaction at a C–C triple bond or cross-coupling at a terminal C–H bond. Combining those reaction patterns could realize a new reaction methodology to synthesize complex molecules including C–C multiple bonds. In this report, we found that the reaction of 3 equivalents of terminal alkyne 1 (aryl substituted alkyne) and an α-bromocarbonyl compound 2 (tertiary alkyl radical precursor) undergoes tandem alkyl radical addition/Sonogashira coupling to produce 1,3-enyne compound 3 possessing a quaternary carbon in the presence of a copper catalyst. Moreover, the reaction of α-bromocarbonyl compound 2 and an alkyne 4 possessing a carboxamide moiety undergoes tandem alkyl radical addition/C–H coupling to produce indolinone derivative 5.


2000 ◽  
Vol 73 (9) ◽  
pp. 2159-2160 ◽  
Author(s):  
Hidenori Kinoshita ◽  
Hirotada Kakiya ◽  
Koichiro Oshima

ChemInform ◽  
2000 ◽  
Vol 31 (51) ◽  
pp. no-no
Author(s):  
Hidenori Kinoshita ◽  
Hirotada Kakiya ◽  
Koichiro Oshima

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