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A Flexible Approach to 6,5‐Benzannulated Spiroketals
Author(s) -
Wilson Zoe E.,
Hubert Jonathan G.,
Brimble Margaret A.
Publication year - 2011
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.201100345
Subject(s) - chemistry , combinatorial chemistry , organic chemistry
A novel route to simple 6,5‐benzannulated spiroketal analogues has been developed. A convergent Horner–Wadsworth–Emmons olefination enabled ready assembly of the spiroketal precursors. Use of a benzyl protecting group strategy enabled an efficient one‐pot hydrogenation/deprotection/spiroketalisation process to be employed providing a robust method to access a range of substituted aromatic monobenzannulated spiroketals.
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