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Volumn 10, Issue 21, 2008, Pages 5023-5026

Lewis acid catalyzed [1,3]-sigmatropic rearrangement of vinyl aziridines

Author keywords

[No Author keywords available]

Indexed keywords

ACID; AZIRIDINE; AZIRIDINE DERIVATIVE; COPPER; PYRROLE DERIVATIVE; PYRROLINE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 58149151106     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol802123e     Document Type: Article
Times cited : (71)

References (42)
  • 37
    • 60949089586 scopus 로고    scopus 로고
    • The substrates in entries 11, 13, and 24 under the thermal conditions form azomethine ylides, and products from these intermediates are observed. In the reactions of entries 19 and 20, the pyrroles can be isolated from the retro-Diels - Alder reaction of the products.
    • The substrates in entries 11, 13, and 24 under the thermal conditions form azomethine ylides, and products from these intermediates are observed. In the reactions of entries 19 and 20, the pyrroles can be isolated from the retro-Diels - Alder reaction of the products.
  • 38
    • 60949098861 scopus 로고    scopus 로고
    • Unfortunately, when compound 1 was synthesized asymmetrically, chirality was not transferred to the product. Compound 1 was transesterified with a chiral alcohol in order to assess enantiomeric purity of the starting material and product. The product was found not to epimerize under the given reaction conditions.
    • Unfortunately, when compound 1 was synthesized asymmetrically, chirality was not transferred to the product. Compound 1 was transesterified with a chiral alcohol in order to assess enantiomeric purity of the starting material and product. The product was found not to epimerize under the given reaction conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.