Quantum chemical CD calculations of dioncophylline A in the solid state
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference53 articles.
1. Asymmetric Total Synthesis of ent-(−)-Roseophilin: Assignment of Absolute Configuration
2. Callipeltoside A: Assignment of Absolute and Relative Configuration by Total Synthesis We thank the National Science Foundation and the National Institutes of Health for their generous support of our programs. OD was supported in part by a fellowship from the Association pour la Recherche contre le Cancer (ARC). J.L.G. was supported in part by a NIH postdoctoral fellowship from the National Cancer Institute. Mass spectra were provided by the Mass Spectroscopy Facility at the University of California, San Francisco supported by the NIH Division of Research Resources, and the Mass Spectrometry Facility at University of California, Irvine. We thank Dr. John Greaves of the latter facility for his assistance.
3. Stereochemical assignment of the fungal metabolite xestodecalactone A by total synthesis
4. A facile degradation procedure for determination of absolute configuration in 1,3-dimethyltetra- and dihydroisoquinolines
5. An improved degradation procedure for determination of the absolute configuration in chiral isoquinoline and β-carboline derivatives
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