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Volumn 55, Issue 4, 2014, Pages 806-810

A novel and diastereoselective construction of H-pyrazolo[3,2-a] isoquinoline fused spirooxindoles via [3+2] cycloaddition This Letter is dedicated with best wishes to Scientist Emeritus Boreddy S.R. Reddy on the occasion of his 65th birthday

(2) Yuvaraj, Panneerselvam a Reddy, Boreddy S R a

a CENTRAL LEATHER RESEARCH INSTITUTE (India)

Author keywords

Cycloaddition; Diastereoselectivity; Pyrazoloisoquinoline; Spirooxindole

Indexed keywords

1,2 DIHYDRO 10' BH SPIRO[INDOLE 3,1' PYRAZOLE [3,2 A] ISOQUINOLINE] 2 CARBOXYLATE; CARBOXYLIC ACID; METHYLENEINDOLINONE; N' (2 ALKYNYLBENZYLIDENE)HYDRAZIDE; OXINDOLE; SILVER; SILVER TRIFLATE; UNCLASSIFIED DRUG; CARBON 13; INDOLE DERIVATIVE; ISOQUINOLINE DERIVATIVE; LEWIS ACID; PYRAZOLE DERIVATIVE; TOLUENE; TRIFLUOROMETHANESULFONIC ACID;

ARTICLE; CATALYST; CHEMICAL STRUCTURE; CROSS LINKING; CYCLIZATION; CYCLOADDITION; DIASTEREOISOMER; DIPOLE; ELIMINATION REACTION; ONE POT SYNTHESIS; ROOM TEMPERATURE; STEREOCHEMISTRY; CARBON NUCLEAR MAGNETIC RESONANCE; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 84892434462 PISSN: 00404039 EISSN: 18733581 Source Type: Journal
DOI: 10.1016/j.tetlet.2013.11.116 Document Type: Article

Times cited : (18)

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