A novel ring system arising from intramolecular oxidative cyclization of 8-(4-pentenyl)dihydroberberine
โ Scribed by Mark Cushman; Donald A. Patrick; Pascal H. Toma; Stephen R. Byrn
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 243 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
An unusual oxidative cyclization reaction was observed in the course of studies on the synthesis of berberine linked to oligonucleotides at the 8position. The novel ring structure of the oxidative cyclization product was confumed using X-ray crystallography.
Our laboratory is investigating general methods for the conjugation of berberine alkaloids to oligonucleotides.
๐ SIMILAR VOLUMES
In a previous paper we have shown that one of the major products of the hypoiodite reaction of cholesterol was 3,4-seco-4-iodo-cholest-5-en-3-al
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
## Abstract Novel 7,8,9,10โtetrahydrothiazolo[5,4โ__a__]acridine and 1,2,3,4โtetrahydroโ12__H__โbenzothiazolo[2,3โ__b__]โquinazolinโ12โone derivatives were synthesized in one step from the corresponding benzothiazoles. These two new tetracyclic skeletons were unambiguously characterized and are pre