✦ LIBER ✦

Transition State Structures of a Dipeptide Related to the Mode of Action of β -lactam Antibiotics

✍ Scribed by Donald B. Boyd

Book ID: 123654586
Publisher: National Academy of Sciences
Year: 1977
Tongue: English
Weight: 865 KB
Volume: 74
Category: Article
ISSN: 0027-8424
DOI: 10.2307/67327

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Intestinal uptake of dipeptides and β-la

Intestinal uptake of dipeptides and β-lactam antibiotics. I. The intestinal uptake system for dipeptides and β-lactam antibiotics is not part of a brush border membrane peptidase

✍ Werner Kramer; Christine Dechent; Frank Girbig; Ulrike Gutjahr; Horst Neubauer 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 893 KB

Diagnosis of nonimmediate reactions to β

Diagnosis of nonimmediate reactions to β-lactam antibiotics

✍ A. Romano; M. Blanca; M. J. Torres; A. Bircher; W. Aberer; K. Brockow; W. J. Pic 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 228 KB

Diversity of the mechanisms of resistanc

Diversity of the mechanisms of resistance to β-lactam antibiotics

✍ Frère, J.-M.; Joris, B.; Granier, B.; Matagne, A.; Jacob, F.; Bourguignon-Bellef 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 353 KB

Synthesis of Novel .beta.-Lactam Core St

Synthesis of Novel .beta.-Lactam Core Structures Related to the Penam and Penem Antibiotics

✍ Ren, Xiao-Feng; Turos, Edward 📂 Article 📅 1994 🏛 American Chemical Society 🌐 English ⚖ 463 KB

Synthesis and reactions of thioaldehyde

Synthesis and reactions of thioaldehyde dehydropeptides related to ?-lactam antibiotics

✍ Cheney, John; Moores, Clive J.; Raleigh, James A.; Scott, A. Ian; Young, Douglas 📂 Article 📅 1974 🏛 The Royal Society of Chemistry 🌐 English ⚖ 197 KB

A Novel Approach to the Synthesis of Pre

A Novel Approach to the Synthesis of Precursors of Tricyclic β-Lactam Antibiotics

✍ Rita Annunziata; Maurizio Benaglia; Mauro Cinquini; Franco Cozzi; Laura Poletti; 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 296 KB 👁 1 views

The stereoselective synthesis of two precursors of tricyclic β-ring-forming reaction followed by the reduction of a functionalized aromatic substituent at C-4 of the β-lactam lactam antibiotics (trinems) has been attempted by a novel approach that involves a highly stereoselective azetidinone nucleu