Journal of Organic Chemistry p. 4227 - 4236 (1988)
Update date:2022-09-26
Topics: Synthesis Enantiospecific Absolute Configuration D-Glyceraldehyde Acetonide
Wagle, Dilip R.
Garai, Chandra
Chiang, Julian
Monteleone, Michael G.
Kurys, Barbara E.
et al.
Optically active 3,4-disubstituted 2-azetidinones have been prepared in good yield by the annelation of Schiff bases from D-glyceraldehyde acetonide with acid chlorides (or equivalent) and triethylamine.The utility of this enantiospecific synthesis was ex
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Doi:10.1021/ja01533a036
()Doi:10.1021/ja01530a044
(1959)Doi:10.1021/ja01524a069
(1959)Doi:10.1039/c2cc18069c
(2012)Doi:10.1021/ol8007183
(2008)Doi:10.1039/c7tb02359f
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