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Volumn 43, Issue 20, 2002, Pages 3781-3782

Aryl epoxide-halohydrin transformations: Stereochemistry of reactions of aryl epoxides with lithium halide-acetic acid reagent

Author keywords

Aryl epoxides; Chlorohydrins; Lithium halides; Stereochemistry

Indexed keywords

1,2,3,4 TETRAHYDROPHTHALEN 1,2 EPOXIDE; 5 METHOXYINDENE OXIDE; 6 METHOXY 1,2,3,4 TETRAHYDROPHTHALEN 1,2 EPOXIDE; ACETIC ACID; EPOXIDE; HALOGEN; INDENE OXIDE; LITHIUM DERIVATIVE; REAGENT; UNCLASSIFIED DRUG;

EID: 0037071220     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)00637-8     Document Type: Article
Times cited : (17)

References (8)
  • 6
    • 84992280582 scopus 로고    scopus 로고
    • 3)
  • 7
    • 84992269844 scopus 로고    scopus 로고
    • 1H NMR absorptions due to the benzylic hydrogens alpha to the halo group. The benzylic C-H absorption that disappeared more rapidly when the halohydrin mixture from each system was treated with base was assigned to the trans halohydrin. The assignment of stereochemistry to the methoxy-substituted halohydrins was based on the assumption that the relative chemical shifts and coupling constants of the benzylic alpha hydrogens parallel the relative chemical shifts and coupling constants of the known cis and trans halohydrins in the parent systems
  • 8
    • 84992232629 scopus 로고    scopus 로고
    • 1H NMR


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.