A convenient regioselective synthesis of spirooxindolinopyrrolizidines incorporating the pyrene moiety through a [3 + 2]-cycloaddition reaction

AbstractA facile one-pot synthesis of spirooxindolinopyrrolizidines incorporating the pyrene moiety was accomplished in good yields through a 1,3-dipolar cycloaddition reaction of 3-aryl-1-(pyren-1-yl)prop-2-en-1-one derivatives with

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

Journal of Heterocyclic Chemistry ◽

10.1002/jhet.5570430631 ◽

2006 ◽

Vol 43 (6) ◽

pp. 1635-1640 ◽

Cited By ~ 13

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

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Facile One-Pot Synthesis of Ferrocene-Based Spiropyrrolidines and Pyrrolizidines Through 1,3-Dipolar Cycloaddition Reaction

Synthetic Communications ◽

10.1080/00397910903243765 ◽

2010 ◽

Vol 40 (15) ◽

pp. 2311-2319 ◽

Cited By ~ 6

Author(s):

A. R. Suresh Babu ◽

R. Raghunathan

Keyword(s):

Cycloaddition Reaction ◽

Dipolar Cycloaddition ◽

One Pot ◽

One Pot Synthesis

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Iodine-mediated $${ sp}^{3}$$ s p 3 C–H functionalization of methyl ketones: a one-pot synthesis of functionalized indolizines via the 1,3-dipolar cycloaddition reaction between pyridinium ylides and ynones

Molecular Diversity ◽

10.1007/s11030-016-9720-9 ◽

2017 ◽

Vol 21 (1) ◽

pp. 1-8 ◽

Cited By ~ 8

Author(s):

Issa Yavari ◽

Jamil Sheykhahmadi ◽

Maryam Naeimabadi ◽

Mohammad Reza Halvagar

Keyword(s):

Cycloaddition Reaction ◽

Dipolar Cycloaddition ◽

Methyl Ketones ◽

One Pot ◽

One Pot Synthesis ◽

Pyridinium Ylides

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

Heterocycles ◽

10.3987/com-93-6596 ◽

1994 ◽

Vol 38 (3) ◽

pp. 587 ◽

Cited By ~ 4

Author(s):

Yoshimitsu Nagao ◽

Kweon Kim ◽

Yoichi Komaki ◽

Shigeki Sano ◽

Masaru Kihara ◽

...

Keyword(s):

Cycloaddition Reaction ◽

Dipolar Cycloaddition ◽

One Pot ◽

One Pot Synthesis

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One-pot synthesis via 1, 3-dipolar cycloaddition reaction to piperazinyl-quinolinyl dispiro heterocyclic derivatives and spectrofluorometric and molecular docking studies on their binding with human serum albumin

Journal of Molecular Structure ◽

10.1016/j.molstruc.2017.08.017 ◽

2017 ◽

Vol 1149 ◽

pp. 439-451 ◽

Cited By ~ 5

Author(s):

Arul Murugesan ◽

Robert Moonsamy Gengan ◽

Ramar Rajamanikandan ◽

Malaichamy Ilanchelian

Keyword(s):

Molecular Docking ◽

Human Serum Albumin ◽

Serum Albumin ◽

Human Serum ◽

Cycloaddition Reaction ◽

Docking Studies ◽

Dipolar Cycloaddition ◽

One Pot ◽

One Pot Synthesis ◽

Heterocyclic Derivatives

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ChemInform Abstract: One-Pot Synthesis of Ethyl-3-aryl-2-(1H-tetrazol-5-yl)acrylates and 3-(1H-Tetrazol-5-yl)coumarins via Tandem [2 + 3] Dipolar Cycloaddition Reaction-Knoevenagel Condensation.

ChemInform ◽

10.1002/chin.201630162 ◽

2016 ◽

Vol 47 (30) ◽

Author(s):

Zahra Jafari Chermahini ◽

Alireza Najafi Chermahini ◽

Hossein A. Dabbagh ◽

Abbas Teimouri

Keyword(s):

Knoevenagel Condensation ◽

Cycloaddition Reaction ◽

Dipolar Cycloaddition ◽

One Pot ◽

One Pot Synthesis

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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

Tetrahedron Letters ◽

10.1016/j.tetlet.2008.11.033 ◽

2009 ◽

Vol 50 (4) ◽

pp. 448-451 ◽

Cited By ~ 25

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

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ChemInform Abstract: An Efficient One Pot Regioselective Synthesis of a 3,3′-Spiro-phosphonylpyrazole-oxindole Framework via Base Mediated [1,3]-Dipolar Cycloaddition Reaction of the Bestmann-Ohira Reagent with Methyleneindolinones.

ChemInform ◽

10.1002/chin.201549089 ◽

2015 ◽

Vol 46 (49) ◽

pp. no-no

Author(s):

Anil M. Shelke ◽

Gurunath Suryavanshi

Keyword(s):

Cycloaddition Reaction ◽

Regioselective Synthesis ◽

Dipolar Cycloaddition ◽

One Pot

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

ChemInform ◽

10.1002/chin.199423152 ◽

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

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An efficient one pot regioselective synthesis of a 3,3′-spiro-phosphonylpyrazole-oxindole framework via base mediated [1,3]-dipolar cycloaddition reaction of the Bestmann–Ohira reagent with methyleneindolinones

Organic & Biomolecular Chemistry ◽

10.1039/c5ob01020a ◽

2015 ◽

Vol 13 (32) ◽

pp. 8669-8675 ◽

Cited By ~ 34

Author(s):

Anil M. Shelke ◽

Gurunath Suryavanshi

Keyword(s):

Cycloaddition Reaction ◽

Regioselective Synthesis ◽

Dipolar Cycloaddition ◽

One Pot

A one pot, highly regioselective synthesis of 3,3′-spiro-phosphonylpyrazole-oxindole by 1,3-dipolar cycloaddition of the Bestmann–Ohira reagent (BOR) & methyleneindolinones has been developed.

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