Tetrahedron Letters p. 635 - 638 (1997)
Update date:2022-08-02
Topics:
Bloodworth
Hagen, Torsten
Johnson, Karen A.
LeNoir, Isabelle
Moussy, Chantal
The versatility of the cyclo-oxymercuriation route to 1,2,4-trioxanes is illustrated by preparing with heterocyclic, unsaturated and carbohydrate substituents and by post-cyclisation modification of the substituents including oxidative cleavage of alkene and reduction, condensation and Wittig olefination of carbonyl groups.
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Doi:10.1021/ja9636350
(1997)Doi:10.1002/(SICI)1521-3765(19990903)5:9<2584::AID-CHEM2584>3.0.CO;2-B
(1999)Doi:10.1016/S0040-4020(98)00088-X
(1998)Doi:10.1016/S0968-0896(96)00270-2
(1997)Doi:10.1016/S0968-0896(96)00273-8
(1997)Doi:10.1016/S0957-4166(97)00047-5
(1997)
