The stereoselective synthesis of cis- and trans-b-lactams via α-amino ester enolates and 1-aza-4-hetero-1,3-butadiene systems. Molecular structure of EtOC(O)C(H)Net2)C(H)(NH)(-t-Bu)C(H)=N(t-Bu)ZnCl2: an unexpectedly isolated intermediate

Koten, G. van; Steen, F.H. van der; Kleijn, H.; Spek, A.L.

The stereoselective synthesis of cis- and trans-b-lactams via α-amino ester enolates and 1-aza-4-hetero-1,3-butadiene systems. Molecular structure of EtOC(O)C(H)Net2)C(H)(NH)(-t-Bu)C(H)=N(t-Bu)ZnCl2: an unexpectedly isolated intermediate

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The stereoselective synthesis of cis- and trans-b-lactams via α-amino ester enolates and 1-aza-4-hetero-1,3-butadiene systems. Molecular structure of EtOC(O)C(H)Net2)C(H)(NH)(-t-Bu)C(H)=N(t-Bu)ZnCl2: an unexpectedly isolated intermediate

Koten, G. van; Steen, F.H. van der; Kleijn, H.; Spek, A.L.

(1991) Journal of organic chemistry, volume 56, issue 20, pp. 5868 - 5875

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ISSN: 0022-3263

Publisher: American Chemical Society

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