Jump to navigation Jump to search
Greek prefixes in alphabetical order indicate ring size:
- α-Lactam (3-atom rings)
- β-Lactam (4-atom rings)
- γ-Lactam (5-atom rings)
- δ-Lactam (6-atom rings)
- ε-Lactam (7-atom rings)
General synthetic methods exist for the organic synthesis of lactams.
- Lactams form by the acid-catalyzed rearrangement of oximes in the Beckmann rearrangement.
- Lactams form from cyclic ketones and hydrazoic acid in the Schmidt reaction.
- Lactams form from cyclisation of amino acids.
- Lactams form from intramolecular attack of linear acyl derivatives from the nucleophilic abstraction reaction.
- In iodolactamization  an iminium ion reacts with a halonium ion formed in situ by reaction of an alkene with iodine.
- Lactams form by copper-catalyzed 1,3-dipolar cycloaddition of alkynes and nitrones in the Kinugasa reaction
- Diels-Alder reaction between cyclopentadiene and chlorosulfonyl isocyanate (CSI) can be utilized to obtain both β- as well as γ-lactam. At lower temp (−78 °C), β-lactam is the preferred product. At optimum temperatures, a highly useful γ-lactam known as Vince Lactam is obtained.
Tautomerization to lactims
- Lactams can polymerize to polyamides.
- Lactone, a cyclic ester.
- β-Lactam antibiotics, which includes penicillins
- Spencer Knapp, Frank S. Gibson Organic Syntheses, Coll. Vol. 9, p.516 (1998); Vol. 70, p.101 (1992) Online article
- Singh, R.; Vince, R. Chem. Rev. 2012, 112 (8), pp 4642–4686."2-Azabicyclo[2.2.1]hept-5-en-3-one: Chemical Profile of a Versatile Synthetic Building Block and its Impact on the Development of Therapeutics"
- Pham, P.-T.; Vince, R. Phosphorus, Sulphur and Silicon 2007, 779-791.
- Media related to Lactams at Wikimedia Commons