Baylis-Hillman carbonates in organic synthesis: A convenient one-pot strategy for nitrone-spiro-oxindole frameworks

Tetrahedron

Volumn 69, Issue 37, 2013, Pages 7995-8001

  Basavaiah, Deevi ^a   Badsara, Satpal Singh ^a   Veeraraghavaiah, Gorre ^a  

^a UNIVERSITY OF HYDERABAD   (India)

Author keywords

Alkylation; Baylis Hillman reaction; Nitrones; Reductive cyclization; Spiro oxindoles

Indexed keywords

CARBONIC ACID DERIVATIVE; ISATIN DERIVATIVE; NITROMETHANE; NITRONE DERIVATIVE; OXINDOLE;

ALKYLATION; ARTICLE; BAYLIS HILLMAN REACTION; CYCLIZATION; ONE POT SYNTHESIS; PRIORITY JOURNAL;

EID: 84880918944     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.07.002     Document Type: Article

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78. One of the referees has suggested to present a brief discussion on characterization of structure of one of the nitrone-spiro-oxindole derivatives using spectral data. This is a very nice suggestion and we thank the referee for the same. Accordingly we present a brief discussion on the characterization of 4a using spectral data.
79. Detailed X-ray crystallographic data is available from the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK for compounds 4a (CCDC # 923595) and 4j (CCDC # 923596).