Differences in the Biological Activity of 2 : 3 : 5 : 6-Tetrachloronitrobenzene and its Isomers
โ Scribed by BROOK, M.
- Book ID
- 109570690
- Publisher
- Nature Publishing Group
- Year
- 1952
- Tongue
- English
- Weight
- 107 KB
- Volume
- 170
- Category
- Article
- ISSN
- 0028-0836
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
1998 separation and purification methods, chromatography separation and purification methods, chromatography V 0200 ## 05 -244 Resolution and Biological Activities of Optical Isomers of 1,4-Diethyl-3,6-epidithiopiperazine-2,5-dione. -The first example of a resolution of a epipolythiopiperazine-2,
The new monomer, a-methoxy-3,6-endo-methylene-1,2,3,6-tetrahydrophthaloyl-5-fluorouracil (MMTFU), was synthesized from 5-fluorouracil (5-FU) and a-methoxy-3,6-endo-methylene-1,2,3,6-tetrahydrophthaloyl chloride (MMTC). Poly (a-methoxy-3,6endo-methylene-1,2,3,6-tetrahydrophthaloyl-5-fluorouracil) [po
The new monomer, โฃ-methoxy-exo-3,6-epoxy-1,2,3,6-tetrahydrophthaloyl-5-fluorouracil (METFU), was synthesized by the reaction of 5-fluorouracil (5-FU) and exo-3,6-epoxy-1,2,3,6-tetrahydrophthalic anhydride (ETA) in order to prepare polymers containing 5-FU moiety. Poly(โฃ-methoxy-exo-3,6-epoxy-1,2,3,6