✦ LIBER ✦

New synthesis of (RS)-carnitine chloride

✍ Scribed by Sharon G. Boots; Marvin R. Boots

Publisher: John Wiley and Sons
Year: 1975
Tongue: English
Weight: 332 KB
Volume: 64
Category: Article
ISSN: 0022-3549
DOI: 10.1002/jps.2600640737

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Refinement of the crystal structure of (

Refinement of the crystal structure of (RS)-carnitine hydrochloride

✍ A. N. Yunuskhodzhaev; EB. Shamuratov; A. S. Batsanov; S. A. Talipov 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 146 KB

Asymmetric synthesis of (R)-(−)-carnitin

Asymmetric synthesis of (R)-(−)-carnitine

✍ Rajendra P Jain; Robert M Williams 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 94 KB

A new synthesis of cyanogen chloride

✍ R. Varma; A.J. Signorelli 📂 Article 📅 1969 🏛 Elsevier Science ⚖ 75 KB

A new, short and efficient synthesis of

A new, short and efficient synthesis of both enantiomers of carnitine

✍ F.D. Bellamy; M. Bondoux; P. Dodey 📂 Article 📅 1990 🏛 Elsevier Science 🌐 French ⚖ 207 KB

## A short, efficient and enantioselective synthesis of both (R) and (S) enantiomers of Carnitine is reported starting with (R) or (S) malic acid and involving a chemoselective reduction step.

A new synthesis of chlorosulfonyl chlori

A new synthesis of chlorosulfonyl chlorides

✍ E. J. Goethals; M. Verzele 📂 Article 📅 2010 🏛 Wiley (John Wiley & Sons) ⚖ 329 KB

y-and a-hydroxyalkane-1-thiols, in many cases easily accessible over the chlorohydrins, are converted to y-and a-chloroalkylsulfonyl chlorides by the combined action of chlorine and water. A mechanism is suggested. This new synthesis method provides an easy way to obtain sultams.

Synthesis of carboxy-labelled l-carnitin

Synthesis of carboxy-labelled l-carnitine

✍ Donald B. Goodfellow; Charles L. Hoppel; Julia S. Turkaly 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 French ⚖ 351 KB

## Abstract A method for the production of carboxy‐labelled l‐carnitine is described. The first step is the chemical synthesis of 4‐N‐trimethylammoniobutanoate (butyrobetaine) from the precursors 4‐aminobutanoate and iodomethane. The second step involves the hydroxylation of butyrobetaine to form l