✦ LIBER ✦

Stereochemical Specificity of Enzymatic Cleavage of β-Phenylserine

✍ Scribed by Gilbert, James B.

Book ID: 126261722
Publisher: American Chemical Society
Year: 1954
Tongue: English
Weight: 275 KB
Volume: 76
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja01645a043

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Enzymatic Cleavage and Synthesis of L-th

Enzymatic Cleavage and Synthesis of L-threo-β-Phenylserine and L-erythro-β-Phenylserine

✍ BRUNS, FRIEDRICH H.; FIEDLER, LISELORE 📂 Article 📅 1958 🏛 Nature Publishing Group 🌐 English ⚖ 218 KB

Synthesis of β-Phenylserines

✍ Wawzonek, S.; Gaffield, W. G. 📂 Article 📅 1963 🏛 American Chemical Society 🌐 English ⚖ 397 KB

Stereochemical specificity of Alzheimer'

Stereochemical specificity of Alzheimer's disease β-peptide assembly

✍ William P. Esler; Evelyn R. Stimson; Jordan B. Fishman; Joseph R. Ghilardi; Harr 📂 Article 📅 1999 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 267 KB

The formation and growth of insoluble amyloid deposits composed primarily of the human ␤-amyloid peptide (A␤) in brain is an essentially invariant feature of Alzheimer's disease (AD) and is widely believed to contribute to the progressive neurodegeneration of the disorder. To probe the specificity o

19. The synthesis of β-phenylserines

✍ Dalgliesh, Charles E. 📂 Article 📅 1949 🏛 The Royal Society of Chemistry ⚖ 503 KB

The Enzymatic Cleavage of β-Carotene: St

The Enzymatic Cleavage of β-Carotene: Still Controversial

✍ George Wolf 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 384 KB

Chemical and enzymatic diastereoselectiv

Chemical and enzymatic diastereoselective cleavage of β-d-galactopyranosylsulfoxides

✍ Noureddine Khiar; Inés Alonso; Natividad Rodriguez; Alfonso Fernandez-Mayoralas; 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 210 KB

The self induced diastereoselective oxidation of several thio-~-D-galactopyranosides to the corresponding sulfoxides, has been shown to occur in high yield. Up to 74% diastereomeric excess could be obtained depending on the structure and the conformation of the starting thioglycoside.Rs and Ss Pheny