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Volumn 62, Issue 11, 1997, Pages 3748-3750

Highly Diastereoselective Epoxidation of Cycloalkenols with Monoperoxyphthalic Acid in Water

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001609736     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9623604     Document Type: Article
Times cited : (33)

References (42)
  • 6
    • 85033148903 scopus 로고    scopus 로고
    • note
    • 11 should be in agreement with a more extensive bond formation at the site adjacent to the heteroatom.
  • 26
    • 85033137626 scopus 로고    scopus 로고
    • 7b
    • 7b
  • 31
    • 85033136671 scopus 로고    scopus 로고
    • 6a
    • 6a
  • 37
    • 85033132473 scopus 로고    scopus 로고
    • 10 The reaction time is not always optimized
    • 10 The reaction time is not always optimized.
  • 38
    • 85033153490 scopus 로고    scopus 로고
    • 7j
    • 7j
  • 40
    • 85033140036 scopus 로고    scopus 로고
    • 6a In strong alkaline medium the transition state of the epoxidation is a bis-anion or a mono-anion depending on the peroxy acid used
    • 6a In strong alkaline medium the transition state of the epoxidation is a bis-anion or a mono-anion depending on the peroxy acid used.
  • 41
    • 85033141657 scopus 로고    scopus 로고
    • 7a
    • 7a
  • 42
    • 4243597363 scopus 로고
    • Wiley: New York; Coll.
    • Böhme H. Organic Synthesis; Wiley: New York, 1955; Coll. Vol. 3, p 619.
    • (1955) Organic Synthesis , vol.3 , pp. 619
    • Böhme, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.