One pot synthesis of novel dispiro[oxindole-thiazolidinedione/thioxo-thiazolidinone/dihydro pyrazolone]-pyrrolidines via 1,3-dipolar cycloaddition reaction of azomethine ylides

2006 ◽  
Vol 43 (6) ◽  
pp. 1635-1640 ◽  
Author(s):  
Shashikanth Ponnala ◽  
Devi Prasad Sahu ◽  
Rishi Kumar ◽  
Prakas R. Maulik
Keyword(s):  
Cycloaddition Reaction ◽  
Azomethine Ylides ◽  
Dipolar Cycloaddition ◽  
One Pot ◽  
One Pot Synthesis

One-Pot Synthesis of New 1,3-Imidazolidines Possessing Three Aryl Groups via a 1,3-Dipolar Cycloaddition Reaction

Heterocycles ◽  
1994 ◽  
Vol 38 (3) ◽  
pp. 587 ◽  
Author(s):  
Yoshimitsu Nagao ◽  
Kweon Kim ◽  
Yoichi Komaki ◽  
Shigeki Sano ◽  
Masaru Kihara ◽  
...  
Keyword(s):  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition ◽  
One Pot ◽  
One Pot Synthesis

A One-Pot Synthesis of Highly Functionalized Indolizines by 1,3-Dipolar Cycloaddition of Azomethine Ylides and Phosphorylated Hydroxyketenimines

Synlett ◽  
2016 ◽  
Vol 27 (18) ◽  
pp. 2601-2605 ◽  
Author(s):  
Issa Yavari ◽  
Maryam Naeimabadi ◽  
Reza Hosseinpour ◽  
Mohammad Halvagar
Keyword(s):  
Azomethine Ylides ◽  
Dipolar Cycloaddition ◽  
One Pot ◽  
One Pot Synthesis

Unexpected one-pot synthesis of new polycyclic coumarin[4,3-c]pyridine derivatives via a tandem hetero-Diels–Alder and 1,3-dipolar cycloaddition reaction

2009 ◽  
Vol 50 (4) ◽  
pp. 448-451 ◽  
Author(s):  
Daman R. Gautam ◽  
John Protopappas ◽  
Konstantina C. Fylaktakidou ◽  
Konstantinos E. Litinas ◽  
Demetrios N. Nicolaides ◽  
...  
Keyword(s):  
Cycloaddition Reaction ◽  
Diels Alder ◽  
Dipolar Cycloaddition ◽  
Pyridine Derivatives ◽  
One Pot ◽  
One Pot Synthesis

ChemInform Abstract: One-Pot Synthesis of New 1,3-Imidazolidines Possessing Three Aryl Groups via a 1,3-Dipolar Cycloaddition Reaction.

ChemInform ◽  
2010 ◽  
Vol 25 (23) ◽  
pp. no-no
Author(s):  
Y. NAGAO ◽  
K. KIM ◽  
Y. KOMAKI ◽  
S. SANO ◽  
M. KIHARA ◽  
...  
Keyword(s):  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition ◽  
One Pot ◽  
One Pot Synthesis

scholarly journals Multicomponent synthesis of spiropyrrolidine analogues derived from vinylindole/indazole by a 1,3-dipolar cycloaddition reaction

2016 ◽  
Vol 12 ◽  
pp. 2893-2897 ◽  
Author(s):  
Manjunatha Narayanarao ◽  
Lokesh Koodlur ◽  
Vijayakumar G Revanasiddappa ◽  
Subramanya Gopal ◽  
Susmita Kamila
Keyword(s):  
Amino Acids ◽  
Cycloaddition Reaction ◽  
Thermal Conditions ◽  
Azomethine Ylides ◽  
Dipolar Cycloaddition ◽  
Side Chains ◽  
Multicomponent Synthesis ◽  
One Pot ◽  
Cyclic Adducts

A new series of spiropyrrolidine compounds containing indole/indazole moieties as side chains have been accomplished via a one-pot multicomponent synthesis. The method uses the 1,3-dipolar cycloaddition reaction between N-alkylvinylindole/indazole and azomethine ylides, prepared in situ from cyclic/acyclic amino acids. The 1,3-dipolar cycloaddition proceeds efficiently under thermal conditions to afford the regio- and stereospecific cyclic adducts.

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