Journal
TETRAHEDRON
Volume 63, Issue 26, Pages 5855-5872Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2007.03.026
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Upon treatment with homochiral lithium (R)-N-benzyl-N-(alpha-methylbenzyl) amide, gamma-benzyloxy but-2-enoates undergo competitive conjugate addition and gamma-deprotonation, while gamma-tert-butyldimethylsilyloxy but-2-enoates undergo exclusive conjugate addition. Treatment of g-benzyloxy or g-tert-butyldimethylsilyloxy but-2-enamides with lithium (R)-N-benzyl-N-(a-methylbenzyl) amide furnishes exclusively the gamma-benzyloxy-or gamma-tert-butyldimethylsilyloxy-beta-amino amide products of conjugate addition in high de. The gamma-tert-butyldimethylsilyloxy-beta-amino butanoate products of conjugate addition readily undergo O-desilylation and concomitant cyclisation to furnish 4-[N-benzyl-N-(alpha-methylbenzyl)amino]-gamma-butyrolactone, which may be stereoselectively functionalised via deprotonation and alkylation to give the corresponding trans-3-alkyl-4-amino-gamma-butyrolactones. Alternatively, stereoselective alkylation of gamma-benzyloxy-or gamma-tert-butyldimethylsilyloxy-beta- amino butanoates and butanamides through enolate formation and alkylation following a tandem (via the (Z)-lithium enolate) or stepwise (via the (E)-lithium enolate) protocol gives a range of separable syn- and anti-alpha-alkyl-beta-amino esters and amides. O-Silyl deprotection of the syn- and anti-alpha-alkyl-beta-amino butanoates with TBAF and concomitant cyclisation provide trans-3-alkyl-4-amino-gamma-butyrolactones, consistent with epimerisation to the thermodynamically favoured trans-lactone occurring upon deprotection. (C) 2007 Elsevier Ltd. All rights reserved.
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