๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Convenient synthesis of N-alkoxymethylbarbituric acids and N-alkoxymethylhydantoins

โœ Scribed by Joseph Gal


Publisher
John Wiley and Sons
Year
1979
Tongue
English
Weight
348 KB
Volume
68
Category
Article
ISSN
0022-3549

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Convenient synthesis of N,N,Nโ€ฒ-trisubsti
โœ John L. Neumeyer ๐Ÿ“‚ Article ๐Ÿ“… 1964 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 172 KB

Toxicity Studies on Triton X 100.-The detergent Triton X 100 at 0.1% concentration was nontoxic when in contact with vegetative forms of bacteria for several hours. The surfactant may be used at room or temperatures of 45 f1' during the membrane washing phase. An additional wash with peptone 0.1% is

N-acylamino acids and peptides I. The sy
โœ H. De Pooter; Haider Ali; C. F. van Sumere ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› Wiley (John Wiley & Sons) โš– 580 KB

## Abstract Procedures for the preparation of Nโ€feruloylglycine (II), โ€DLโ€alanine (XX), โ€DLโ€valine (XXII) and โ€Lโ€leucine (XXIV) by classical methods are proposed and compared. The spectral characteristics and Rfโ€values of the substances are included. The compounds were synthesized because Nโ€feruloy

Convenient Synthesis of N-Trimethylsilyl
โœ Bernd Wrackmeyer; Jรผrgen Weidinger; Wolfgang Milius ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ German โš– 116 KB ๐Ÿ‘ 2 views

Bis(N-trimethylsilylamino)plumbylenes 1 {[Me 3 Si(R)N] 2 Pb with R = t Bu (a), Me 3 Si (b), 9-(9-borabicyclo[3.3.1]nonyl) (c)} react smoothly with an excess of TiCl 4 to give PbCl 2 and N-trimethylsilylaminotitanium trichlorides 3 aยฑc. In contrast, the analoguous reaction of the corresponding stanny

Synthesis of N-tert-Butyloxycarbonyl- an
โœ Dr.-Ing. B. Rzeszotarska; Mgr. S. Wiejak ๐Ÿ“‚ Article ๐Ÿ“… 1968 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 233 KB ๐Ÿ‘ 1 views

residue is treated with ice. The aqueous suspension is extracted with benzene (about 300 ml), and the organic phase is at once chromatographed on acid A1203. Benzene (1000 ml) is used for elution. After evaporation of the solvent the residue is taken up in ether, and the solution is decanted at once