Diversity-oriented approach to linearly fused spirocycles via strategic utilization of a [2+2+2] cycloaddition and the Diels-Alder reaction

Tetrahedron

Volumn 71, Issue 10, 2015, Pages 1597-1603

  Kotha, Sambasivarao ^a   Ali, Rashid ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY BOMBAY   (India)

Author keywords

Active methylene compounds; Diels Alder reaction; Spirocycles; Sultine derivatives; Wilkinson's catalyst; 2+2+2 Cycloaddition

Indexed keywords

ALKADIENE; TETRABUTYLAMMONIUM;

AROMATIZATION; ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLOADDITION; DEHYDROGENATION; LINEARLY FUSED SPIROCYCLE; MOLECULAR LIBRARY; PRIORITY JOURNAL;

ALNUS;

EID: 84923095923     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2015.01.009     Document Type: Article

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