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Volumn 5, Issue 3, 1999, Pages 834-844

Wagner-Meerwein rearrangements in the gas phase: Anchimeric assistance to acid-induced dissociation of optically active phenylpropanols

Author keywords

Anchimeric assistance; Chirality; Gas phase chemistry; Phenonium ions; Stereochemistry

Indexed keywords

PHENYL GROUP; PROPANOL;

EID: 0032988539     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3765(19990301)5:3<834::AID-CHEM834>3.0.CO;2-G     Document Type: Article
Times cited : (10)

References (54)
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    • 0001656937 scopus 로고    scopus 로고
    • 18O incorporation in 1s is interpreted in terms of the intermolecular 2s→1s isomerization mechanism, shown in path ii)→iii) of Scheme 4.
    • (1998) J. Org. Chem. , vol.63 , pp. 1020
    • Speranza, M.1    Troiani, A.2
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    • note
    • 3, neutralization of the O-protonated ethers, arising from addition of Ir, IV r, and IV s to methanol, may proceed through several pathways, including proton transfer to the substrate itself, to the walls of the reaction vessel, or to adventitious bases, either initially added to the gaseous mixture or formed from its radiolysis.
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    • note
    • H+, are taken equal to unity. The validity of this assumption is demonstrated in the following paper.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.