Scheme 1. Strategy for the synthesis of (Γ)-galanthamine.
Total synthesis of (+)-pedamide. A new, remote controlled asymmetric induction
β Scribed by Mitsutoshi Yanagiya; Fuyuhiko Matsuda; Kazuo Hasegawa; Takeshi Matsumoto
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 247 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Total synthesis of optically active pedamlde 2, one of the tetrahydropyran moieties of the potent insect poison pederlne A, was achieved by employing a new, remote controlled asymmetric reduction of a ketone as key step.
π SIMILAR VOLUMES
A total synthesis of pamamycin 607 1 is described. The synthesis of the C(1)-C(18) fragment involved the tin(IV) chloride-promoted reaction between (3R)-3-(N-methyl)tosylaminohexanal 18 and the allylstannane 4 followed by cyclisation and reductive removal of the phenylselanyl group to give the tetra
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v