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Volumn 69, Issue 10, 2004, Pages 3359-3367

Kinetics and Mechanism of Hydrolysis of N-Acyloxymethyl Derivatives of Azetidin-2-one

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; DERIVATIVES; ESTERS; HYDROLYSIS; MOLECULAR STRUCTURE; PH EFFECTS; REACTION KINETICS;

EID: 2442475244     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0358123     Document Type: Article
Times cited : (16)

References (48)
  • 37
    • 0003464216 scopus 로고    scopus 로고
    • NIST Standard Reference Database No. 69
    • March
    • a values nor proton affinities (PAs) are available for esters of 2-methoxybenzoic, phenylacetic, or cinnamic acids. However, methyl esters of 3- and 4-methoxybenzoic acids have higher PAs than methyl benzoate, as do the esters of all methyl-substituted benzoic acids, which leads us to assume that the methyl ester of 2-methoxybenzoic acid will have a higher PA than methyl benzoate. Similarly, the PA of methyl 2-butenoate is greater than that for methyl butanoate, suggesting that the PA for methyl cinnamate will be greater than that for methyl benzoate.)
    • (2003) NIST Chemistry WebBook
  • 38
    • 2442496146 scopus 로고    scopus 로고
    • See ref 15, p 109
    • See ref 15, p 109.
  • 40
    • 2442460897 scopus 로고    scopus 로고
    • note
    • 2OH, assuming that azetidin-2-one exerts the same electronic effect that of N-methylacetamido moiety (σ* = 2.25). See ref 15.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.