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Regioselective Synthesis of Fluorinated Phenols, Biaryls, 6 H ‐Benzo[ c ]chromen‐6‐ones and Fluorenones Based on Formal [3+3] Cyclizations of 1,3‐Bis(silyl enol ethers)
Author(s) -
Hussain Ibrar,
Yawer Mirza Arfan,
Lau Matthias,
Pundt Thomas,
Fischer Christine,
Görls Helmar,
Langer Peter
Publication year - 2008
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200700887
Subject(s) - regioselectivity , chemistry , silylation , enol , phenols , silyl enol ether , enol ether , medicinal chemistry , stereochemistry , organic chemistry , catalysis
A variety of fluorinated phenols, biaryls, 6 H ‐benzo[ c ]chromen‐6‐ones and fluorenones were prepared based on regioselective [3+3] cyclizations of 1,3‐bis(silyl enol ethers) with 2‐fluoro‐3‐silyloxy‐2‐en‐1‐ones. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)