scholarly journals Convenient one-step Synthesis of Substituted Pyrano[2,3-c]isoquinoline (2-amino-4H-chromenes) via three Component Reaction between Alkyl isocyanides and Dialkyl Acetylenedicarboxylate in the presence of 3-Hydroxyisoquinoline

2010 ◽  
Vol 6 (1) ◽  
pp. 873-877
Author(s):  
Bita Mohtat ◽  
Shahla Salmani ◽  
Amineh Aminian ◽  
Hoorieh Djahaniani

The reactive intermediate generated by the addition of alkyl isocyanides to dialkyl acetylenedicarboxylate are trapped by 3-hydroxyisoquinoline to produce highly functionalized 4H-chromenes in 83-92% yields.

2007 ◽  
Vol 2007 (10) ◽  
pp. 602-604 ◽  
Author(s):  
Mohammad Anary-Abbasinejad ◽  
Hossain Anaraky-Ardakani ◽  
Forough Rastegari ◽  
Alireza Hassanabadi

The reactive intermediate generated by the reaction of alkyl isocyanides and dialkyl acetylenedicarboxylates was trapped by 4-phenylaminocoumarin to produce dialkyl 2-cyclohexylamino-5-oxo-4 H,5 H-pyrano[3,2- c]chromene-3,4-dicarboxylates in good yields.


2017 ◽  
Vol 57 (2) ◽  
Author(s):  
Bita Mohtat ◽  
Saeedeh Farsijani ◽  
Maryam Razaghi ◽  
Hoorieh Djahaniani

The reactive intermediate generated by the addition of <em>tert</em>-butyl and 1,1,3,3-tetramethyl butyl isocyanide to dialkyl acetylenedicarboxylate was trapped by 7-hydroxycoumarin to produce highly functionalized 4<em>H</em>-chromenes in fairly good yields. When the reaction is performed with cyclohexyl isocyanide, 1-azabuta-1,3-dienes were obtained.


2011 ◽  
Vol 22 (7) ◽  
pp. 771-773 ◽  
Author(s):  
Bita Mohtat ◽  
Hoorieh Djahaniani ◽  
Issa Yavari ◽  
Masomeh G. Dehbalaei ◽  
Saba A. Jam

Synthesis ◽  
2018 ◽  
Vol 50 (20) ◽  
pp. 4097-4103 ◽  
Author(s):  
Shufeng Chen ◽  
Xin-Xing Wu ◽  
Chenjun Wang ◽  
Wanrong Zhao ◽  
Haiying Zhao

A palladium-catalyzed three-component intermolecular aryl­etherification reaction of ferrocene-substituted allenes, aryl iodides and phenols or alcohols is reported. In this three-component reaction, two new C–C and C–O bonds are formed in one step with high regio- and stereoselectivity. The high selectivity obtained in this reaction can be attributed to the steric effect of the bulky ferrocene group.


2011 ◽  
Vol 35 (11) ◽  
pp. 661-663 ◽  
Author(s):  
Alireza Hassanabadi ◽  
Mohammad H. Mosslemin ◽  
Sonia Singh ◽  
Seyyed Ali Shaterchi

2007 ◽  
Vol 2007 (8) ◽  
pp. 455-457 ◽  
Author(s):  
Mohammad Anary-Abbasinejad ◽  
Alireza Hassanabadi ◽  
Hossein Anaraki-Ardakani

Three-component reaction between acetylenic esters, aldehyde semicarbazones and tributyl- or triethyl phosphite leads to stable crystalline phosphite ylides at one step in nearly quantitative yields.


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