An Extension of the Wittig Reaction: Attack of Phosphorus Ylides at Acyl Groups in Organocobalt Complexes

2007 ◽  
Vol 26 (27) ◽  
pp. 6805-6811 ◽  
Author(s):  
Qibao Wang ◽  
Hongjian Sun ◽  
Shimin Fang ◽  
Mingcui Liu ◽  
Klaus Harms ◽  
...  
ChemInform ◽  
2014 ◽  
Vol 45 (52) ◽  
pp. no-no
Author(s):  
Yi-Ling Tsai ◽  
Siang-en Syu ◽  
Shu-Mei Yang ◽  
Utpal Das ◽  
Yu-Shiou Fan ◽  
...  

2010 ◽  
Vol 16 (25) ◽  
pp. 7376-7379 ◽  
Author(s):  
Wen-Bo Liu ◽  
Hu He ◽  
Li-Xin Dai ◽  
Shu-Li You

2012 ◽  
Vol 476-478 ◽  
pp. 1218-1221
Author(s):  
Jian Hong Jia ◽  
Hua Qing Dong ◽  
Yu Jin Li ◽  
Wei Jian Sheng ◽  
Jian Rong Gao

One-pot process for preparation ferrocenylethene derivatives by solvent-free Wittig Reaction of ferrocenecarboxaldehyde, alcohol, triphenylphosphonium bromide, and NaOH without the synthesis of phosphorus ylides was reported. The ferrocenylethene products obtained had an 80% yield with NaOH as the base at room temperature for 30 to 90 minutes.


2002 ◽  
Vol 124 (22) ◽  
pp. 6244-6245 ◽  
Author(s):  
Viktor P. Balema ◽  
Jerzy W. Wiench ◽  
Marek Pruski ◽  
Vitalij K. Pecharsky

ChemInform ◽  
2010 ◽  
Vol 33 (44) ◽  
pp. no-no
Author(s):  
Viktor P. Balema ◽  
Jerzy W. Wiench ◽  
Marek Pruski ◽  
Vitalij K. Pecharsky

2011 ◽  
Vol 13 (16) ◽  
pp. 4176-4179 ◽  
Author(s):  
Aijun Lin ◽  
Junying Wang ◽  
Haibin Mao ◽  
Huiming Ge ◽  
Renxiang Tan ◽  
...  

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