✦ LIBER ✦

Synthesis of (2RS)-[3-13C]- and (2RS)-[3-14C] leucine

✍ Scribed by Panayiotis Anastasis; Karl Overton; Sheo Bux Singh

Publisher: John Wiley and Sons
Year: 1984
Tongue: French
Weight: 284 KB
Volume: 21
Category: Article
ISSN: 0022-2135
DOI: 10.1002/jlcr.2580210502

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of (2S,4S)-[5-13C] leucine, (2

Synthesis of (2S,4S)-[5-13C] leucine, (2R,4S)-[5-13C] leucine, and (2RS)-[1,2-13C2] leucine

✍ D. John Aberhart; Bruce H. Weiller 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 French ⚖ 256 KB 👁 1 views

SYNTHESIS OF (2s , 4S)-[5-l 3C] LEUC INE , (2R ,4S)-[5-' 3C] LEUC I NE , AND (2RS)-[1 ,2-13C,] LEUCINE D. John Aberhart\* and Bruce H. W e i l l e r The Worcester Foundation f o r Experimental B i o l o g y Shrewsbury, Massachusetts 01545 SUMMARY (2RSY3S)-[4-13 ClVal i n e was d i a z o t i z e d an

Synthesis of (3RS)-[2,3-3H2 (N)]-β-leuci

Synthesis of (3RS)-[2,3-3H2 (N)]-β-leucine

✍ D. John Aberhart; Horng-Jau Lin 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 French ⚖ 278 KB

Syntheses nouvelles de la mevalonolacton

Syntheses nouvelles de la mevalonolactone marquee AU 14C, 13C, - (RS) mevalonolactone (14C2-4,5) et (RS) mevalonolactone (14C-5)

✍ Bernard Rousseau; Jean-Pierre Beaucourt; Louis Pichat 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 French ⚖ 440 KB

MEVALONOLACTONE (14c,5) e t ( RS) MEVALONOLACTONE ( I 4 c -5 ) . Bernard ROUSSEAU, Jean-Pierre BEAUCOURT, Louis PICHAT\* S e r v i c e des Molecules Marquees -CEN-SACLAY -F. 91191 GIF-SUR-YVETTE Cedex Three new routes t 3 (RS) mvalonolactone s u i t a b l e for the double labeling w i t h i s o t

Isotopically labelled tropane alkaloids.

Isotopically labelled tropane alkaloids. The synthesis of (RS)-[3′, 3′-2H2]- and (RS)-[1′-13C, 3′, 3′-2H2]- hyoscyamines for metabolism studies in plants

✍ Stephen Patterson; David O'Hagan 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 101 KB

## Abstract A synthetic route to isotopically labelled forms of the tropane alkaloid hyoscyamine, including (__RS__)‐[3′, 3′,‐^2^H~2~]‐ (**2a**) and (__RS__)‐[1′‐^13^C, 3′, 3′,‐^2^H~2~]‐ (**2b**) hyoscyamines, involving the reaction between phenylacetyl tropine and formaldehyde is described. The is

Microwave-assisted synthesis of (RS) met

Microwave-assisted synthesis of (RS) methyl-2-([2′-14C]4,6-dimethoxypyrimidin-2′-yloxy)-2-phenyl [1-14C]ethanoate

✍ K. M. Mathew; S. Ravi; V. K. P. Unny; N. Sivaprasad 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 French ⚖ 121 KB

We report here a facile synthesis of (RS) methyl-2-([2 0 -14 C]4,6-dimethoxypyrimidin-2 0yloxy)-2-phenyl [1-14 C]ethanoate under microwave irradiation.

Synthesis of methyl [2-13C-2,2-d2]- and

Synthesis of methyl [2-13C-2,2-d2]- and [3-13C-3,3-d2]tetracosanoate

✍ J. George Pomonis; Heldur Hakk 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 French ⚖ 331 KB