✦ LIBER ✦

The stepwise synthesis of methyl α-isomaltooligoside derivatives and methyl α-isomaltopentaoside

✍ Scribed by Ronald Eby; Conrad Schuerch

Book ID: 108308416
Publisher: Elsevier Science
Year: 1976
Tongue: English
Weight: 949 KB
Volume: 50
Category: Article
ISSN: 0008-6215
DOI: 10.1016/s0008-6215(00)83852-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Novel synthesis of Nα-methyl-arginine an

Novel synthesis of Nα-methyl-arginine and Nα-methyl-ornithine derivatives

✍ Chu-Biao Xue; William F. DeGrado 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 270 KB

Synthesis of 3α-Chlorinated Methyl Litho

Synthesis of 3α-Chlorinated Methyl Lithocholate Derivatives.

✍ Lutfun Nahar; Satyajit D. Sarker; Alan B. Turner 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 16 KB

Studies on the Synthesis of Disaccharide

Studies on the Synthesis of Disaccharides: II. The Synthesis of Methyl α-Vicianoside and Methyl α-Primeveroside

✍ Elizabeth E. Lee, J. P. O'Donoghue and E. O'Brien 📂 Article 📅 1975 🏛 Royal Irish Academy ⚖ 559 KB

Synthesis of α-[14C]methyl and α-[3H]met

Synthesis of α-[14C]methyl and α-[3H]methyl-L-tryptophan

✍ T. K. Venkatachalam; S. Mzengeza; M. Diksic 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 French ⚖ 383 KB

## Abstract The title compounds were synthesized starting from dimethyl (2S,3aR,8aS)‐(+)‐8‐(phenylsulfonyl)hexahydrophyrrolo[2,3‐b]indole‐1,2‐dicarboxylate. This compound on treatment with LDA followed by reaction with [^14^C]methyl iodide or [^3^H]methyl iodide gave the methyl substituted derivati

α-Methyl-α-chloro-β-propiothiolactone in

α-Methyl-α-chloro-β-propiothiolactone in the synthesis of derivatives of thioglycidic acid

✍ M. G. Lin'kova; A. M. Orlov; O. V. Kil'disheva; I. L. Knunyants 📂 Article 📅 1969 🏛 Springer 🌐 English ⚖ 452 KB

Synthesis of α-alkyl and α-functionalize

Synthesis of α-alkyl and α-functionalized methyl-α-amino acids

✍ P. Bey; J.P. Vevert 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 186 KB

As part of our program aimed at the design of specific enzyme inhibitors, we have been interested in the synthesis of a-alkyl substituted-u-amino acids of type 1 (Y -H or heteroatom functions). R CH3 The classical route to a-alkyl substituted-a-amino acids consists of a Bucherer or a Strecker reacti