An efficient Benzannulation protocol for the synthesis of 9,9-Diphenyl-9H -fluorenols using Intramolecular Allene Friedel-Crafts Annulation-Reference-Cited by-同舟云学术

An efficient Benzannulation protocol for the synthesis of 9,9-Diphenyl-9H -fluorenols using Intramolecular Allene Friedel-Crafts Annulation

Published:2019-08-12 Issue:33 Volume:2019 Page:5740-5748
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Yaragorla Srinivasarao¹^ORCID,Rajesh P.¹

Affiliation:

1. School of Chemistry; Gurbaksh Building, W-16, 17; University of Hyderabad; P.O. Central University, Gachibowli 5000046 Hyderabad Telangana State India

Funder

Science and Engineering Research Board

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201900895/fullpdf

Reference45 articles.

1. Mimicking the biological activity of diazobenzo[b]fluorene natural products with electronically tuned diazofluorene analogs

2. 3-(3′-Fluorenyl-9′-oxo)-l-alanine: a novel photoreactive conformationally constrained amino acid

3. 2,7-Disubstituted Amidofluorenone Derivatives as Inhibitors of Human Telomerase

4. Iron III ‐catalyzed Chemoselective Cycloaromatization Reactions for the synthesis of 5‐Brominated Benzo[ b ]fluorenones

5. A General Synthetic Route to Indenofluorene Derivatives as New Organic Semiconductors

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