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Stereocontrolled Routes to Bridged Ethers by Tandem Cyclizations
Author(s) -
Marson Charles M.,
Campbell Jon,
Hursthouse Michael B.,
Malik K. M. Abdul
Publication year - 1998
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/(sici)1521-3773(19980504)37:8<1122::aid-anie1122>3.0.co;2-o
Subject(s) - domino , octane , tandem , electrophile , chemistry , contraction (grammar) , ring (chemistry) , stereochemistry , medicinal chemistry , organic chemistry , biology , materials science , catalysis , composite material , endocrinology
Ring contraction of a 3,4‐epoxyalcohol, then lactolization and electrophilic attack are the steps in the domino cyclization protocol for the formation of 8‐oxabicyclo[3.2.1]octane systems [Eq. (a)].