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Volumn 51, Issue 34, 1995, Pages 9385-9392

Cycloaddition reactions of 5H,7H-thiazolo[3,4-c] oxazolium-1-oxides with imines

Author keywords

[No Author keywords available]

Indexed keywords

7 THIA 2,5 DIAZASPIRO[3,4]OCTANE DERIVATIVE; IMIDAZO[1,5 C]THIAZOLE DERIVATIVE; IMIDAZOLE DERIVATIVE; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0029135031     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(95)00545-J     Document Type: Article
Times cited : (34)

References (23)
  • 11
    • 84916470541 scopus 로고    scopus 로고
    • Fr. Pat. 2,539,417 1984, C.A. 102:45932w.
  • 13
    • 37049105216 scopus 로고
    • Assessment of racemisation in N-alkylated amino-acid derivatives during peptide coupling in a model dipeptide system
    • 3), is the only formed when we used the N-formyl-(R)-thiazolidine- 4-carboxylic acid as starting material (1, R-H). Attempts to carry out the cyclodehydration step at lower temperature (0–5 ° C) did not lead to cycloaddition products probably owing to the non-formation of (α):
    • (1981) Journal of the Chemical Society, Perkin Transactions 1 , pp. 2982
    • Davies1    Mohammed2
  • 18
    • 0013520177 scopus 로고
    • This first step was supposed to occur in the thermal rearrangement of monocyclic 3-acylamino-β-lactams:, and references therein
    • (1966) Tetrahedron , vol.22 , pp. 2489
    • Bird1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.