𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and oxidative cleavage of the major equilibrium products of ascomycin and FK 506

✍ Scribed by K Baumann; B Oberhauser; M.A Grassberger; G Haidl; G Schulz


Publisher
Elsevier Science
Year
1995
Tongue
French
Weight
205 KB
Volume
36
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Synthesis of ascomycin and FK 506 deriva
✍ Peter Nussbaumer; Maximilian A. Grassberger; Gerhard Schulz πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 205 KB

Oxidation of the 22-hydrazone of ascomycin using manganese dioxide generates in situ the reactive 22-diazo intermediate, which decomposes to give ascomycin analogues with modified effector region. In dichloromethane several products are obtained, whereas in methanol a cyclopropane derivative is gene

1H, 13C, and 15N assignments and seconda
✍ Robert X. Xu; David Nettesheim; Edward T. Olejniczak; Robert Meadows; Gerd Gemme πŸ“‚ Article πŸ“… 1993 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 998 KB

## Abstract The ^1^H, ^13^C, and ^15^N resonances of FKBP when bound to the immunosuppressant, ascomycin, were assigned using a computer‐aided analysis of heteronuclear double and triple resonance three‐dimensional nmr spectra of [U‐^15^N] FKBP/ascomycin and [U‐^15^N, ^13^C] FKBP/ascomycin. In addi