메뉴 건너뛰기




Volumn 16, Issue 2, 2014, Pages 452-455

Stereoselective capture of n-acyliminium ions generated from a-hydroxy-n-acylcarbamides: Direct synthesis of uracils from barbituric acids enabled by smi2 reduction

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; AMINOALCOHOL; BARBITURIC ACID; BARBITURIC ACID DERIVATIVE; DRUG DERIVATIVE; IMINE; ION; LEWIS ACID; URACIL;

EID: 84896693030     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol403340j     Document Type: Article
Times cited : (13)

References (44)
  • 26
    • 84896761180 scopus 로고    scopus 로고
    • α-Hydroxy-Nacylcarbamides were prepared using SmI2-H2O (dr 77:23 to 91:9). The stereochemistry at the hemiaminal center has no bearing on the stereochemical outcome of the additions
    • α-Hydroxy-Nacylcarbamides were prepared using SmI2-H2O (dr 77:23 to 91:9). The stereochemistry at the hemiaminal center has no bearing on the stereochemical outcome of the additions.
  • 27
    • 0346787791 scopus 로고    scopus 로고
    • Reviews On SmI2
    • Reviews on SmI2: (a) Kagan, H. B. Tetrahedron 2003, 59, 10351.
    • (2003) Tetrahedron , vol.59 , pp. 10351
    • Kagan, H.B.1
  • 35
    • 84880994816 scopus 로고    scopus 로고
    • Deuterated drugs
    • Deuterated drugs: (a) Katsnelson, A. Nat. Med 2013, 19, 656.
    • (2013) Nat. Med , vol.19 , pp. 656
    • Katsnelson, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.