pectively (e.g. for (2a) in CC14: v, , (CSj) = 1146vw, vs(CS2) = 61 9 cm-1 vs). Spectroscopic and X-ray data indicate pseudooctahedral environment of the metal in (/a)--( 2f) with (pseudo)-Czv symmetry. The IH-NMR spectra indicate in particular that an isomeric mixture containing (Ze) and a tolyldit
Synthesis of 3′-Amido-3′-deoxyadenosine 3′,5′-Cyclo-phosphate
✍ Scribed by Dipl.-Chem. Michael Morr; Dr. Maria-Regina Kula; Dipl.-Chem. Georg Roesler; Prof. Dr. Bernd Jastorff
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 248 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0044-8249
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📜 SIMILAR VOLUMES
Additivity of alkyl substituent effects was assumed in that work. [4] The NMR spectra were obtained in the Fourier transform mode, at 25.2 MHz. using a Varian XL-100 instrument with a variable temperature probe. [ 5 ] Acid A is well over lo' times stronger than acid B. 161 The solution in acid B p
Cyclophane 1, a compound we have long sought""' and one of the final target molecules in the field of [3,3]cyclophane chemistry, has finally been synthesized and characterized. We expect 1 to have fascinating chemical and structural features. A photochemical isomerization of 1 to the propella[3,]prt