Chemistry of andrographolide: formation of novel di-spiropyrrolidino and di-spiropyrrolizidino-oxindole adducts via one-pot three-component [3+2] azomethine ylide cycloaddition

Tetrahedron Letters

Volumn 51, Issue 12, 2010, Pages 1585-1588

  Hazra, Abhijit ^a   Paira, Priyankar ^a   Sahu, Krishnendu B ^a   Naskar, Subhendu ^a   Saha, Pritam ^a   Paira, Rupankar ^a   Mondal, Shyamal ^a   Maity, Arindam ^a   Luger, Peter ^b   Weber, Manuela ^b   Mondal, Nirup B ^a   Banerjee, Sukdeb ^a  

^a INDIAN INSTITUTE OF CHEMICAL BIOLOGY   (India)

^b FREIE UNIVERSITÄT BERLIN   (Germany)

Author keywords

2D NMR; Andrographolide; Azomethine ylide; Dipolar cycloaddition; Dispiro oxindole

Indexed keywords

AMINO ACID; ANDROGRAPHOLIDE; AZOMETHINE YLIDE; ISATIN DERIVATIVE; OXINDOLE; PROLINE; PYRROLIDINE DERIVATIVE; SARCOSINE; SPIRO COMPOUND;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL BOND; CONJUGATION; CYCLOADDITION; DIPOLE; NUCLEAR OVERHAUSER EFFECT; ONE POT SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; X RAY CRYSTALLOGRAPHY;

EID: 76649091565     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.01.052     Document Type: Article

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