58277-26-2Relevant articles and documents
Studies towards the total synthesis of batzelladine A
Elliott, Mark C.,Long, Matthew S.
, p. 2003 - 2011 (2007/10/03)
Application of a diastereoselective three-component coupling to the bicyclic core of the batzelladine alkaloids is described. The synthesis features the elaboration of glutamic acid by use of Eschenmoser sulfide contraction. An earlier approach is also included, which shows some limitations of dithiane chemistry when applied to the particular compounds required for this target.
A Chemoenzymatic Synthesis of (R)-2-(1-Hydroxyethyl)-2,3-dithiane
Bracher, Franz,Litz, Thomas
, p. 555 - 559 (2007/10/03)
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Lewis acid mediated addition of 2-acyl-1,3-dithianes to α,β-unsaturated ketones: Synthesis of cyclohexenedione mono-dithioacetals
Bulman Page, Philip C.,Marchington, Allan P.,Graham, Lisa J.,Harkin, Shaun A.,Wood, William W.
, p. 10369 - 10386 (2007/10/02)
2-Acyl-1,3-dithianes undergo Lewis acid-mediated conjugate addition to α,β-unsaturated ketones to provide 1,5-diketones which suffer base-catalyzed intramolecular aldol reaction to produce monodithioacetals of cyclohex-2-en-1,4-diones and cyclohex-3-en-1,