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Volumn 58, Issue 26, 2002, Pages 5327-5333

Reactions of hydroxylated sodium nitronates with acetic anhydride/pyridine

Author keywords

Acetic nitronic anhydrides; Nitro compounds; Nitronate salts

Indexed keywords

ACID ANHYDRIDE; HYDROXYL GROUP; NITRO DERIVATIVE; NITROALKANE; PYRIDINE DERIVATIVE;

EID: 0037167071     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)00487-8     Document Type: Article
Times cited : (5)

References (27)
  • 17
    • 0005915903 scopus 로고    scopus 로고
    • The ease of the acetylation of primary hydroxyl group, together with the long distance between the hydroxyl and the nitrogen may be responsible for the lack of isoxazoline-N-oxide.
  • 18
    • 0005955976 scopus 로고    scopus 로고
    • Hydroxamic acid derivatives as 15 have been detected, or isolated, in reactions between either primary nitroalkanes or their nitronate salts with acylating agents, such as acetyl chlorides and acid anhydrides. Several mechanisms to justify their formation are given in Refs. 2, 3
  • 27
    • 0005986260 scopus 로고    scopus 로고
    • A similar attack of HO-5 on C-1 of the hypothetic acetic nitronic anhydride from 23a would explain the formation of the 1,5-lactone oxime 27a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.