메뉴 건너뛰기




Volumn 9, Issue 22, 2007, Pages 4651-4653

Synthesis of tertiary α-hydroxy acids by silylene transfer to α-keto esters

Author keywords

[No Author keywords available]

Indexed keywords

ESTER; HYDROXYACID;

EID: 35948971695     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702148x     Document Type: Article
Times cited : (34)

References (39)
  • 2
    • 35948965328 scopus 로고    scopus 로고
    • Hanessian, S. Total Synthesis of Natural Products. The Chiron Approach; Pergamon: New York, 1983; Chaper 2.
    • (b) Hanessian, S. Total Synthesis of Natural Products. The Chiron Approach; Pergamon: New York, 1983; Chaper 2.
  • 32
    • 35948988984 scopus 로고    scopus 로고
    • Details are provided as Supporting Information
    • Details are provided as Supporting Information.
  • 33
    • 35948988202 scopus 로고    scopus 로고
    • Chelation-controlled Ireland-Claisen rearrangements proceed with moderate to high diastereoselectivity: (a) ref 3c
    • Chelation-controlled Ireland-Claisen rearrangements proceed with moderate to high diastereoselectivity: (a) ref 3c.
  • 36
    • 35949001355 scopus 로고    scopus 로고
    • 1H NMR spectroscopy. These materials are likely to be isomers because the compound exhibits satisfactory elementary analysis.
    • 1H NMR spectroscopy. These materials are likely to be isomers because the compound exhibits satisfactory elementary analysis.
  • 37
    • 0038695134 scopus 로고    scopus 로고
    • The relative stereochemistry of the product was assigned based upon analogies to similar systems: Nubbemeyer, U
    • The relative stereochemistry of the product was assigned based upon analogies to similar systems: Nubbemeyer, U. Synthesis 2003, 961-1008.
    • (2003) Synthesis , pp. 961-1008


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.