Synthesis of Novel Taxol Analogues and Evaluation of Their Biological Activities. -Two novel title compounds (IV), (X), are found to be weakly cytotoxic against J774.2 cells. -(WENDER,
Synthesis of a Biologically Active Taxol Analogue
β Scribed by Prof. Dr. Siegfried Blechert; Andrea Kleine-Klausing
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 367 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
β¦ Synopsis
us compare the C-C bonds in butadiene (8, Frame 21), and acrolein (9, Frame 22). The illustrations present ELF values in a plane lying 1 Bohr above the plane of the nuclei and intersecting the x-bonding region, and show that the x component of the C-C bond is larger in 9 than it is in 8. H, 3 H, ,H Fe F H, ,C=C -H o=c, ,c=c -H F-CI@ ++F-&
π SIMILAR VOLUMES
## Abstract 1. The extent of racemization and the coupling yield in peptide synthesis were studied under high dilution conditions. The azide method yielded the best results. 2. Five linear pentaβpeptide precursors related to gramicidin S were subjected to cyclization in order to study how the diffe