The synthesis and reactions of a monocyclic β-lactam tripeptide, 1-[(1R)-carboxy-2-methylpropyl]- (3R -[(5S-5-amino- 5-carboxypentanamido]-(4R)-mercaptoazetidin-2-one, a putative intermediate in penicillin biosynthesis

MLA

Leslie D. Field, et al. “The Synthesis and Reactions of a Monocyclic β-Lactam Tripeptide, 1-[(1R)-Carboxy-2-Methylpropyl]- (3R -[(5S-5-Amino- 5-Carboxypentanamido]-(4R)-Mercaptoazetidin-2-One, a Putative Intermediate in Penicillin Biosynthesis.” Tetrahedron, vol. 40, Jan. 1984, pp. 1907–18. EBSCOhost, https://doi.org/10.1016/s0040-4020(01)91148-2.

APA

Leslie D. Field, Jack E. Baldwin, Gamini S. Jayatilake, Michael John Crimmin, John J. Usher, Sir Edward P. Abraham, Robert L. White, & Robert M. Adlington. (1984). The synthesis and reactions of a monocyclic β-lactam tripeptide, 1-[(1R)-carboxy-2-methylpropyl]- (3R -[(5S-5-amino- 5-carboxypentanamido]-(4R)-mercaptoazetidin-2-one, a putative intermediate in penicillin biosynthesis. Tetrahedron, 40, 1907–1918. https://doi.org/10.1016/s0040-4020(01)91148-2

Chicago

Leslie D. Field, Jack E. Baldwin, Gamini S. Jayatilake, Michael John Crimmin, John J. Usher, Sir Edward P. Abraham, Robert L. White, and Robert M. Adlington. 1984. “The Synthesis and Reactions of a Monocyclic β-Lactam Tripeptide, 1-[(1R)-Carboxy-2-Methylpropyl]- (3R -[(5S-5-Amino- 5-Carboxypentanamido]-(4R)-Mercaptoazetidin-2-One, a Putative Intermediate in Penicillin Biosynthesis.” Tetrahedron 40 (January): 1907–18. doi:10.1016/s0040-4020(01)91148-2.