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) | Zendy

Hussain Ibrar | Zendy; Yawer Mirza Arfan | Zendy; Lau Matthias | Zendy; Pundt Thomas | Zendy; Fischer Christine | Zendy; Görls Helmar | Zendy; Langer Peter | Zendy

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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)

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