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Volumn 133, Issue 10, 1996, Pages 951-964

Phosphorothioate-mercaptophosphonate rearrangement: Synthesis of new o-mercaptoaryl-and omercaptoheteroaryl phosphonates and their derivatives

Author keywords

1,3 sigma tropic rearrangement; O mercaptoarylphosphonate; O mercaptoheteroarylphosphonate; Ortho lithiation; Phosphorothioate

Indexed keywords


EID: 33746307004     PISSN: 00378968     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (25)

References (76)
  • 4
    • 0018620062 scopus 로고
    • a) Boezi JA, Phann Ther (1979) 4, 231 b) Obcrg B, ibid (1983) 19, 387
    • (1979) Phann Ther , vol.4 , pp. 23
    • Boezi, J.A.1
  • 32
    • 33746280319 scopus 로고
    • Morisson DC, ibid
    • b) Morisson DC, ibid (1955) 77, 181
    • (1955) , vol.77 , pp. 181
  • 37
    • 0026757038 scopus 로고
    • a) Bianchetti G, Rend ist lombardo sei PI I (1957) 91, 68 (Chem Abstr (1958) 52, 11769b) b) Liu DD, Chen DW, Chen ZC, Synth Commun (1992) 22, 2903
    • (1957) Rend Ist Lombardo Sei PI I , vol.91 , pp. 68
    • Bianchetti, G.1
  • 54
    • 33746290822 scopus 로고
    • van Keulen BJ, Kellogg RM, Piepers O, ibid
    • b) van Keulen BJ, Kellogg RM, Piepers O, ibid (1979) 285
    • (1979) , pp. 285
  • 61
    • 33746283740 scopus 로고
    • a) Redmore D, US3 770 750 (1973) (Chem Abstr (1974) 80, 37285z)
    • (1973) US3 770 750 , vol.1974 , pp. 80
    • Redmore, D.1
  • 62
    • 33746277875 scopus 로고
    • b) Redmore D, US3 786 055 (1974) (Chem Abstr (1Q74) 80, 96154d)
    • (1974) US3 786 055 , vol.174 , pp. 80
    • Redmore, D.1
  • 63
    • 33746283740 scopus 로고
    • Redmore D, US3 775 057 (1973) (Chem Abstr (1974) 80, 147521f)
    • (1973) US3 775 057 , vol.1974 , pp. 80
    • Redmore, D.1
  • 70
    • 33746302030 scopus 로고    scopus 로고
    • 1H NMR (CDC13): 7.71 (dd, H5, 3Jnp = 8.6 Hz, 4JHP = 4.4 Hz)). The formation of this product can be explained by a second orfAo-lithiation on the thienyl ring after the rearrangement followed by a nucleophilic attack on the starting S-thienylphosphorothioate 14a. (Figure Presented)
    • 1H NMR (CDC13): 7.71 (dd, H5, 3Jnp = 8.6 Hz, 4JHP = 4.4 Hz)). The formation of this product can be explained by a second orfAo-lithiation on the thienyl ring after the rearrangement followed by a nucleophilic attack on the starting S-thienylphosphorothioate 14a. (Figure Presented)
  • 71
    • 33746277591 scopus 로고    scopus 로고
    • For the preparation of diisopropyl phosphorochloridate see
    • For the preparation of diisopropyl phosphorochloridate see:
  • 74
    • 33746312731 scopus 로고    scopus 로고
    • For the preparation of 4,4'-oxydi(benzenethiol) see
    • For the preparation of 4,4'-oxydi(benzenethiol) see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.