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Volumn 121, Issue 33, 1999, Pages 7720-7721

Chiral SEM ether-tin tetrachloride as an enantioselective hydroxymethylating reagent for silyl enol ethers: γ-Effect of silicon [13]

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL; REAGENT; SILANE DERIVATIVE; SILICON; STANNIC CHLORIDE;

EID: 0033603863     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9916613     Document Type: Letter
Times cited : (24)

References (23)
  • 1
    • 0005866813 scopus 로고
    • While far from efficient, there is nevertheless a report on the enantioselective hydroxymethylation. Fujii, M.; Sato, Y.; Aida, T.; Yoshihara, M. Chem. Express 1992, 7, 309.
    • (1992) Chem. Express , vol.7 , pp. 309
    • Fujii, M.1    Sato, Y.2    Aida, T.3    Yoshihara, M.4
  • 9
    • 0345238512 scopus 로고    scopus 로고
    • note
    • Although the reaction of 1 with p-methoxybenzyl ether of (R)-BINOL-tin tetrachloride at -40°C for 5 h gave the desired d-benzyl ketone in 58% yield, no asymmetric induction was observed.
  • 16
    • 33644516158 scopus 로고
    • and references therein
    • 2: Paterson, I. Tetrahedron 1988, 44, 4207 and references therein.
    • (1988) Tetrahedron , vol.44 , pp. 4207
    • Paterson, I.1
  • 18
    • 0003955355 scopus 로고    scopus 로고
    • CRC Press: Boca Raton, Chapter 4
    • The possibility of an unsymmetrical structure, in which two oxygen atoms in a single MOM group of 2a are coordinated to the tin atom, was clearly denied. Santelli, M.; Pons, J.-M. Lewis Acids and Selectivity in Organic Synthesis; CRC Press: Boca Raton, 1996; Chapter 4.
    • (1996) Lewis Acids and Selectivity in Organic Synthesis
    • Santelli, M.1    Pons, J.-M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.