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Volumn 48, Issue 13, 2007, Pages 2357-2359

Preparation of N-alkyl-N′-carboalkoxy guanidines: unexpected effective trans-alkoxylation transforming the 2,2,2-trichloroethoxycarbonyl into various carbamates

Author keywords

Carbamate; Guanidine; Trans alkoxylation

Indexed keywords

2,2,2 TRICHLOROETHOXYCARBONYL; ALCOHOL; AMIDINE; AMINE; AMMONIA; BUTYLOXYCARBONYL 1H PYRAZOLE 1 CARBOXAMIDINE; CARBAMIC ACID DERIVATIVE; CARBONYL DERIVATIVE; GUANIDINE DERIVATIVE; N METHYLBENZYL N' TERT BUTYLOXYCARBONYLGUANIDINE; THIOUREA; UNCLASSIFIED DRUG;

EID: 33847328305     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.01.126     Document Type: Article
Times cited : (9)

References (20)
  • 1
    • 33847305282 scopus 로고    scopus 로고
    • Durant, G. J.; Colin, E. J., Charon, R. U.S. Patent 3,950,333, 1976, CAN 85:33015.
  • 7
    • 15444365617 scopus 로고    scopus 로고
    • For a recent review, see: and references cited therein
    • For a recent review, see:. Katritzky A.R., and Rogovoy B.V. ARKIVOC iv (2005) 49-87 and references cited therein
    • (2005) ARKIVOC , vol.iv , pp. 49-87
    • Katritzky, A.R.1    Rogovoy, B.V.2
  • 15
    • 0028361429 scopus 로고
    • 3): δ 1.51 (s, 9H), 1.57 (s, 9H), 6.44 (dd, J = 2.7 and 1.7 Hz, 1H), 7.64 (d, J = 1.7 Hz, 1H), 8.32 (d, J = 2.7 Hz, 1H), 8.94 (br s, 1H). See Ref.:
    • 3): δ 1.51 (s, 9H), 1.57 (s, 9H), 6.44 (dd, J = 2.7 and 1.7 Hz, 1H), 7.64 (d, J = 1.7 Hz, 1H), 8.32 (d, J = 2.7 Hz, 1H), 8.94 (br s, 1H). See Ref.:. Drake B., Patek M., and Lebl M. Synthesis (1994) 579-582
    • (1994) Synthesis , pp. 579-582
    • Drake, B.1    Patek, M.2    Lebl, M.3
  • 17
    • 33847273437 scopus 로고    scopus 로고
    • note
    • 4a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.