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Volumn 16, Issue 20, 2014, Pages 5278-5281

Developing Pd(II) catalyzed double sp3 C-H alkoxylation for synthesis of symmetric and unsymmetric acetals

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EID: 84908254800     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol502377x     Document Type: Article
Times cited : (35)

References (55)
  • 48
    • 84908244361 scopus 로고    scopus 로고
    • note
    • When the temperature was raised up to 120°C, the major product was the dialkoxylation product, with a trace amount of the monoalkoxylation compound.
  • 55
    • 84908229958 scopus 로고    scopus 로고
    • note
    • The submission of the purified symmetrical acetals (Figure 2) to conditions described for the formation of unsymmetrical acetals only results in a small amount of unsymmetrical acetals (for more details, please see SI). This observation supports our proposed mechanism that the reaction does favor a sequential double C-H alkoxylation procedure, but not another pathway such as potential acetal exchange.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.