In this paper we described the synthesis of the cis-2-azabicyclo[3.3.0]octane derivative (5b) employing highly diastereoselective mercury(II)-mediated intramolecular amino-cyclization, followed by reductive demercuration of ethyl erythro-1allyl-2-amino-1-cyclopentanecarboxylate (7b). Molecular dynam
Hypotensive Agents. X. 3-Azabicyclo[3.3.0]octane Derivatives1,2
β Scribed by RICE, LEONARD M.; GROGAN, CHARLES H.
- Book ID
- 115545819
- Publisher
- American Chemical Society
- Year
- 1959
- Tongue
- English
- Weight
- 630 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0022-3263
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## 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
Enantiopure 2-azabicyclo[3.3.0]octanes 1a-d and ent-1e pure compounds (2c,d and ent-2e). The structure of compounds 2a and ent-2e was confirmed by an X-ray study. were oxidized with mCPBA to provide either diastereomeric pairs of N-oxides (2a/3a and 2b/3b) or diastereomerically The factors that affe