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Concerted and stepw...
Concerted and stepwise solvolytic elimination and substitution reactions: Stereochemistry and substituent effects
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- Meng, QS (author)
- Uppsala universitet
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- Gogoll, Adolf (author)
- Uppsala universitet,Avdelningen för organisk kemi
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- Thibblin, Alf (author)
- Uppsala universitet
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(creator_code:org_t)
- 1997-02-12
- 1997
- English.
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In: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 119:6, s. 1217-1223
- Related links:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Subject headings
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- 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
- NATURVETENSKAP -- Kemi -- Organisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Organic Chemistry (hsv//eng)
Keyword
- PROMOTED E2 REACTION; AQUEOUS SOLVENT; BASE CATALYSIS; ION-PAIRS; MECHANISMS; DEPROTONATION; SPECTROSCOPY; DERIVATIVES; BORDERLINE; E1CB
- Kemi
- Chemistry
Publication and Content Type
- ref (subject category)
- art (subject category)
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