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- Meng, QSUppsala universitet (author)
Concerted and stepwise solvolytic elimination and substitution reactions: Stereochemistry and substituent effects
- Article/chapterEnglish1997
Publisher, publication year, extent ...
- 1997-02-12
- American Chemical Society (ACS),1997
- printrdacarrier
Numbers
- LIBRIS-ID:oai:DiVA.org:uu-80759
- https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-80759URI
- https://doi.org/10.1021/ja962469tDOI
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- Language:English
- Summary in:English
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Notes
- Addresses: UNIV UPPSALA, INST CHEM, S-75121 UPPSALA, SWEDEN.
- Solvolysis of the R,R and R,S isomers 2a-X and 2b-X, respectively, (X = I, Br, OBs) in 25 vol % acetonitrile in water gives the elimination products 4, 5a, and 5b along with the substitution products 2a-OH, 2b-OH, 2a-NHCOMe, and 2b-NHCOMe. The rates of e
Subject headings and genre
- NATURVETENSKAP Kemi Organisk kemi hsv//swe
- NATURAL SCIENCES Chemical Sciences Organic Chemistry hsv//eng
- PROMOTED E2 REACTION; AQUEOUS SOLVENT; BASE CATALYSIS; ION-PAIRS; MECHANISMS; DEPROTONATION; SPECTROSCOPY; DERIVATIVES; BORDERLINE; E1CB
- Kemi
- Chemistry
Added entries (persons, corporate bodies, meetings, titles ...)
- Gogoll, AdolfUppsala universitet,Avdelningen för organisk kemi(Swepub:uu)adolfgog (author)
- Thibblin, AlfUppsala universitet (author)
- Uppsala universitetAvdelningen för organisk kemi (creator_code:org_t)
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- In:Journal of the American Chemical Society: American Chemical Society (ACS)119:6, s. 1217-12230002-78631520-5126
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