메뉴 건너뛰기




Volumn 9, Issue 10, 1998, Pages 1641-1644

A new highly enantioselective synthesis of both (R)- and (S)-2- mercaptosuccinic acids

Author keywords

[No Author keywords available]

Indexed keywords

2 MERCAPTOSUCCINIC ACID; SUCCINIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032557502     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(98)00149-9     Document Type: Article
Times cited : (14)

References (22)
  • 3
    • 0002984046 scopus 로고
    • Vashi, B. S.; Mehta, D. S.; Shah, V. H. Indian J. Chem. 1995, 34B, 802. Desai, K.; Baxi, A. J. J. Indian Chem. Soc. 1992, 69, 212.
    • (1992) Indian Chem. Soc. , vol.69 , pp. 212
    • Desai, K.1    Baxi, A.J.J.2
  • 10
    • 0344883705 scopus 로고
    • Nozaki, K.; Yoshihara, M.; Matsubara, Y.; Maeshima, T. Phosphorus and Sulfur 1985, 22, 1. Okuda, Y.; Yoshihara, M.; Maeshima, T.; Amaya, N.; Murata, Y. Chem. Express 1989, 4, 13; Chem. Abstr. 1989, 111, 232021.
    • (1989) Chem. Abstr. , vol.111 , pp. 232021
  • 11
    • 0345314854 scopus 로고
    • Yukagaku
    • Ninoi, T.; Yoshihara, M.; Maeshima, T.; Fujii, M.; Aida, T. Yukagaku 1988, 37, 1044; Chem. Abstr. 1989, 111, 114715. Nozaki, K.; Yoshihara, M.; Matsubara, Y.; Maeshima, T. Yukagaku 1984, 33, 797; Chem. Abstr. 1985, 102, 113911.
    • (1988) , vol.37 , pp. 1044
    • Ninoi, T.1    Yoshihara, M.2    Maeshima, T.3    Fujii, M.4    Aida, T.5
  • 12
    • 0344883704 scopus 로고
    • Ninoi, T.; Yoshihara, M.; Maeshima, T.; Fujii, M.; Aida, T. Yukagaku 1988, 37, 1044; Chem. Abstr. 1989, 111, 114715. Nozaki, K.; Yoshihara, M.; Matsubara, Y.; Maeshima, T. Yukagaku 1984, 33, 797; Chem. Abstr. 1985, 102, 113911.
    • (1989) Chem. Abstr. , vol.111 , pp. 114715
  • 13
    • 0345314850 scopus 로고
    • Yukagaku
    • Ninoi, T.; Yoshihara, M.; Maeshima, T.; Fujii, M.; Aida, T. Yukagaku 1988, 37, 1044; Chem. Abstr. 1989, 111, 114715. Nozaki, K.; Yoshihara, M.; Matsubara, Y.; Maeshima, T. Yukagaku 1984, 33, 797; Chem. Abstr. 1985, 102, 113911.
    • (1984) , vol.33 , pp. 797
    • Nozaki, K.1    Yoshihara, M.2    Matsubara, Y.3    Maeshima, T.4
  • 14
    • 0344020659 scopus 로고
    • Ninoi, T.; Yoshihara, M.; Maeshima, T.; Fujii, M.; Aida, T. Yukagaku 1988, 37, 1044; Chem. Abstr. 1989, 111, 114715. Nozaki, K.; Yoshihara, M.; Matsubara, Y.; Maeshima, T. Yukagaku 1984, 33, 797; Chem. Abstr. 1985, 102, 113911.
    • (1985) Chem. Abstr. , vol.102 , pp. 113911
  • 18
    • 0344883703 scopus 로고    scopus 로고
    • 3OD) δ 7.20-7.58 (m, 15H), 4.89 (bs, 2H), 3.22 (dd, J=3.7, 11.1 Hz, 1H), 2.41 (dd, J=11.1, 17.3 Hz, 1H), 1.42 (dd, J=17.3, 3.7 Hz, 1H)
    • 3OD) δ 7.20-7.58 (m, 15H), 4.89 (bs, 2H), 3.22 (dd, J=3.7, 11.1 Hz, 1H), 2.41 (dd, J=11.1, 17.3 Hz, 1H), 1.42 (dd, J=17.3, 3.7 Hz, 1H).
  • 19
    • 0345314853 scopus 로고    scopus 로고
    • The enantiomeric excesses of 3 and 5 were determined by chiral HPLC using a Chiralcel OJ-R column from Daicel Chemical Industries, Ltd
    • The enantiomeric excesses of 3 and 5 were determined by chiral HPLC using a Chiralcel OJ-R column from Daicel Chemical Industries, Ltd.
  • 21
    • 0344451907 scopus 로고    scopus 로고
    • 3OD) δ 4.96 (bs, 2H), 4.68 (m, 2H), 2.75-3.1 (m, 3H), 1.42 (t, J=7.2 Hz, 3H)
    • 3OD) δ 4.96 (bs, 2H), 4.68 (m, 2H), 2.75-3.1 (m, 3H), 1.42 (t, J=7.2 Hz, 3H).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.