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Volumn , Issue 9, 2000, Pages 1423-1428

The suitability of anion-accelerated oxy-Cope rearrangement as a probe to study πi-facial selectivity. An experimental study with (6-methyl-1-oxa-4-thiaspiro[4.5]dec-6-en-7-yl)(allyl)methanols

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE; DISSOCIATION; NEGATIVE IONS; SOLVENTS; STEREOCHEMISTRY;

EID: 0034616464     PISSN: 14704358     EISSN: None     Source Type: Journal    
DOI: 10.1039/a909839i     Document Type: Article
Times cited : (3)

References (57)
  • 19
  • 36
    • 33645905817 scopus 로고    scopus 로고
    • One of the referees suggested that the 18a: 18b (R = Ph) ratio be determined by analytical HPLC or GC. However, since the separation of the multiplets is very clear cut, the authors feel that this may not be warranted
    • One of the referees suggested that the 18a: 18b (R = Ph) ratio be determined by analytical HPLC or GC. However, since the separation of the multiplets is very clear cut, the authors feel that this may not be warranted.
  • 37
    • 33645910292 scopus 로고    scopus 로고
    • note
    • w = 0.049.
  • 57
    • 33645946134 scopus 로고    scopus 로고
    • Allyl phenyl ketone was prepared from the pyridinium chlorochromate (PCC) oxidation of 1-phenylbut-3-en-1-ol which, in turn, was prepared from the reaction of PhMgBr with, acrolein following standard methods.
    • Allyl phenyl ketone was prepared from the pyridinium chlorochromate (PCC) oxidation of 1-phenylbut-3-en-1-ol which, in turn, was prepared from the reaction of PhMgBr with, acrolein following standard methods.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.