Synthesis and x-ray crystal structure determination of 1, 3-bridged. beta.-lactams: novel, anti-Bredt. beta.-lactams

…, BH Lee, MM Miller, OP Anderson

Index: Williams; Lee; Miller; Anderson Journal of the American Chemical Society, 1989 , vol. 111, # 3 p. 1073 - 1081

Full Text: HTML

Citation Number: 53

Abstract

Abstract: The first successful syntheses of several anti-Bredt P-lactams from alkyl acetoacetate in 1 1-14 steps are described. The key cyclization reaction involves the Rh (I1)- catalyzed carbene insertion of the diazo derivatives 12, 23, and 31 into the NH bond of the 0- lactams. These (f)-1, 3-bridged 0-lactams have IR absorptions of 1780-1 795 cm-'for the (3- lactam carbonyls. The structure of 32d has been determined by X-ray crystallography; this ...

Related Articles:

Chemo-and diastereoselective reduction of. beta.-enamino esters: A convenient synthesis of both cis-and trans-. gamma.-amino alcohols and. beta.-amino esters

[Bartoli; Cimarelli; Marcantoni; Palmieri; Petrini Journal of Organic Chemistry, 1994 , vol. 59, # 18 p. 5328 - 5335]

Lanthanoid Triflate Catalyzed Conjugate Addition of Amines to. ALPHA.,. BETA.-Unsaturated Esters. A Facile Route to Optically Active. BETA.-Lactam.

[Matsubara, Seijiro; Yoshioka, Masahito; Utimoto, Kiitiro Chemistry Letters, 1994 , # 5 p. 827 - 830]

GABA-uptake inhibitors: construction of a general pharmacophore model and successful prediction of a new representative

[N'Goka; Schlewer; Linget; Chambon; Wermuth Journal of Medicinal Chemistry, 1991 , vol. 34, # 8 p. 2547 - 2557]

Lanthanoid Triflate Catalyzed Conjugate Addition of Amines to. ALPHA.,. BETA.-Unsaturated Esters. A Facile Route to Optically Active. BETA.-Lactam.

[Matsubara, Seijiro; Yoshioka, Masahito; Utimoto, Kiitiro Chemistry Letters, 1994 , # 5 p. 827 - 830]

More Articles...