Reaction Between Isocyanides and Dialkyl Acetylenedicarboxylates in the Presence of 4,5-Diphenyl-1,3-dihydro-2H-imidazol-2-one. One-Pot Synthesis of 5H-Imidazo[2,1-b][1,3]oxazine Derivatives.

ChemInform ◽  
2005 ◽  
Vol 36 (29) ◽  
Author(s):  
Mehdi Adib ◽  
Khadijeh Ghanbary ◽  
Manizheh Mostofi ◽  
Hamid Reza Bijanzadeh
Keyword(s):  
One Pot ◽  
Dialkyl Acetylenedicarboxylates ◽  
One Pot Synthesis ◽  
Oxazine Derivatives

scholarly journals A New and Efficient One-pot Synthesis of Trialkyl 6-tert-Butylamino-2H-pyran-2-one-3,4,5-tricarboxylates

1999 ◽  
Vol 23 (6) ◽  
pp. 368-369
Author(s):  
Issa Yavari ◽  
Abbas Ali Esmaili ◽  
Sakineh Asghari ◽  
Hamid Reza Bijanzadeh
Keyword(s):  
One Pot ◽  
Tert Butyl ◽  
Dialkyl Acetylenedicarboxylates ◽  
One Pot Synthesis ◽  
High Yields

The highly reactive 1:1 intermediate produced in the reaction between tert-butyl isocyanide and dialkyl acetylenedicarboxylates is trapped by dialkyl 2-bromomalonates to yield the title compounds in fairly high yields.

Ultrasound-assisted one-pot synthesis of 1,3-oxazine derivatives catalysed by BF3–SiO2 under neat conditions

2012 ◽  
Vol 36 (7) ◽  
pp. 398-401 ◽  
Author(s):  
Mudumala Veeranarayana Reddy ◽  
Kwon Taek Lim ◽  
Jong Tae Kim ◽  
Yeon Tae Jeong
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Ultrasound Assisted ◽  
Oxazine Derivatives

scholarly journals A Facile Synthesis of Polysubstituted Pyrroles by One-Pot Three-Component Reaction

2012 ◽  
Vol 9 (4) ◽  
pp. 2239-2244 ◽  
Author(s):  
Hossein Anaraki-Ardakani ◽  
Maziar Noei ◽  
Mina Karbalaei-Harofteh ◽  
Shahab Zomorodbakhsh
Keyword(s):  
Room Temperature ◽  
Facile Synthesis ◽  
One Pot ◽  
Pyrrole Derivatives ◽  
Dialkyl Acetylenedicarboxylates ◽  
One Pot Synthesis ◽  
Three Component Reaction ◽  
High Yields ◽  
Neutral Conditions

A new and efficient one-pot synthesis of polysubstituted pyrrole derivatives by three-component reaction between dialkyl acetylenedicarboxylates, triphenylphosphine, 2-aminopyridin derivatives in the presence of arylglyoxals is described. The reactions were performed in dichloromethane at room temperature and neutral conditions and afforded high yields of products.

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