An efficient palladium catalyzed stereocontrolled synthesis of 4a-angular methyl substituted hydrofluorenes

Article abstract of DOI:10.1080/00397919508015849

A high yield stereoselective synthesis of 4a-angularly methyl substituted cis-hexahydrofluorenes 5a-h and tetrahydrofluorenes 7a,b has been developed by palladium-catalyzed intramolecular Heck-type cyclization of the respective exo-olefins 4a-h and 4a,b t

Full text of DOI:10.1080/00397919508015849

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Synthetic Communications: An
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Organic Chemistry
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An Efficient Palladium
Catalyzed Stereocontrolled
Synthesis of 4a-Angular Methyl
Substituted Hydrofluorenes
Jayanta K. Mukhopadhyaya a , Sitaram Pal a & Usha
Ranjan Ghatak a
a Department of Organic Chemistry , Indian
Association for the Cultivation of Science , Jadavpur,
Calcutta, 700 032, India
Published online: 23 Sep 2006.
To cite this article: Jayanta K. Mukhopadhyaya , Sitaram Pal & Usha Ranjan Ghatak
(1995) An Efficient Palladium Catalyzed Stereocontrolled Synthesis of 4a-Angular
Methyl Substituted Hydrofluorenes, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 25:11, 1641-1657,
DOI: 10.1080/00397919508015849
To link to this article: http://dx.doi.org/10.1080/00397919508015849
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