Conformational studies (1,2) of the cyclic sulfites of 2-substituted-propane-1,3-dials have indicated that these esters occupy preferentially a chair form with axial S=O bond. X-ray analyses (3,4) of two compounds have shown that the sulfite group holds the remainder of the ring in au almost ideal s
Intramolecular nucleophilicSN2 substitution at the tetrahedral carbon atom: Anab initiostudy
✍ Scribed by R. M. Minyaev; V. I. Minkin
- Publisher
- Springer
- Year
- 1999
- Tongue
- English
- Weight
- 813 KB
- Volume
- 48
- Category
- Article
- ISSN
- 1573-9171
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📜 SIMILAR VOLUMES
Whereas reaction of trans-2-chloro or 2-bromo-3-tert-butyloxirane with thiophenc Zate occuï>s at C-3 to gi7>e 2-phenylmercapto-3,3-dimethyZbutanaZ,phenoZates give substitution at C-2 witk retention of tke oxirane ring and retention of configuration witk kinetics tkat indicate a bimoZecuZar meckanism
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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 “Full Text” option. The original article is trackable v