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Volumn 65, Issue 18, 2000, Pages 5834-5836

Highly efficient selective monohydrolysis of symmetric diesters

Author keywords

[No Author keywords available]

Indexed keywords

ESTER DERIVATIVE; SOLVENT;

EID: 0033832846     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0001986     Document Type: Note
Times cited : (79)

References (28)
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    • (1963) Organic Synthesis , vol.4 , pp. 417
    • Strube, R.E.1
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    • and references therein
    • (f) Ward, R. S. Chem. Soc. Rev. 1990, 19, 1 and references therein.
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    • Ward, R.S.1
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    • note
    • In most cases, the dicarboxylic acids, which may form in the reaction, stayed in the aqueous layer after extraction with ethyl acetates.
  • 16
    • 0010430624 scopus 로고
    • This "conformational lock" due to electrostatic interaction between carboalkoxy groups and other functional groups to explain diastereoselectivity has been reported. For example, see: (a) Yamamoto, Y.; Nemoto, H.; Kikuchi, R.; Komatsu, H.; Suzuki, I. J. Am. Chem. Soc. 1990, 112, 8598. (b) Yamamoto, Y.; Taniguchi, K.; Maruyama, K. J. Chem. Soc., Chem. Commun. 1985, 1429. (c) Yamamoto, Y.; Chounan, Y, Nishii, S.; Ibuka, T.; Kitabara, H. J. Am. Chem. Soc. 1992, 114, 7652.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 8598
    • Yamamoto, Y.1    Nemoto, H.2    Kikuchi, R.3    Komatsu, H.4    Suzuki, I.5
  • 17
    • 37049097504 scopus 로고
    • This "conformational lock" due to electrostatic interaction between carboalkoxy groups and other functional groups to explain diastereoselectivity has been reported. For example, see: (a) Yamamoto, Y.; Nemoto, H.; Kikuchi, R.; Komatsu, H.; Suzuki, I. J. Am. Chem. Soc. 1990, 112, 8598. (b) Yamamoto, Y.; Taniguchi, K.; Maruyama, K. J. Chem. Soc., Chem. Commun. 1985, 1429. (c) Yamamoto, Y.; Chounan, Y, Nishii, S.; Ibuka, T.; Kitabara, H. J. Am. Chem. Soc. 1992, 114, 7652.
    • (1985) J. Chem. Soc., Chem. Commun. , pp. 1429
    • Yamamoto, Y.1    Taniguchi, K.2    Maruyama, K.3
  • 18
    • 0001562620 scopus 로고
    • This "conformational lock" due to electrostatic interaction between carboalkoxy groups and other functional groups to explain diastereoselectivity has been reported. For example, see: (a) Yamamoto, Y.; Nemoto, H.; Kikuchi, R.; Komatsu, H.; Suzuki, I. J. Am. Chem. Soc. 1990, 112, 8598. (b) Yamamoto, Y.; Taniguchi, K.; Maruyama, K. J. Chem. Soc., Chem. Commun. 1985, 1429. (c) Yamamoto, Y.; Chounan, Y, Nishii, S.; Ibuka, T.; Kitabara, H. J. Am. Chem. Soc. 1992, 114, 7652.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 7652
    • Yamamoto, Y.1    Chounan, Y.2    Nishii, S.3    Ibuka, T.4    Kitabara, H.5
  • 19
    • 0033551748 scopus 로고    scopus 로고
    • 7b,c (a) Niwayama, S.; Inouye, Y.; Eastman, M. Tetrahedron Lett. 1999, 40, 5961. (b) Battiste, M. A.; Griggs, B. G.; Sacktt, D.; Coxon, J. M.; Steel, P. J. J. Organomet. Chem. 1987, 330, 437. (c) Dahl, L. F.; Wei, C. H. Inorg. Chem. 1963, 4, 71
    • (1999) Tetrahedron Lett. , vol.40 , pp. 5961
    • Niwayama, S.1    Inouye, Y.2    Eastman, M.3
  • 21
    • 0009559617 scopus 로고
    • 7b,c (a) Niwayama, S.; Inouye, Y.; Eastman, M. Tetrahedron Lett. 1999, 40, 5961. (b) Battiste, M. A.; Griggs, B. G.; Sacktt, D.; Coxon, J. M.; Steel, P. J. J. Organomet. Chem. 1987, 330, 437. (c) Dahl, L. F.; Wei, C. H. Inorg. Chem. 1963, 4, 71
    • (1963) Inorg. Chem. , vol.4 , pp. 71
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    • note
    • Half-ester 1b is a known compound, but the melting point was not found.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.