메뉴 건너뛰기




Volumn 32, Issue 5, 2011, Pages 1741-1744

Diisopropyl L-malate as a new chiral auxiliary for dynamic kinetic resolution of α-bromo esters and asymmetric syntheses of aminoflavones and dihydroquinoxalinones

Author keywords

Asymmetric synthesis; Chiral auxiliary; Dynamic kinetic resolution; Flavonoids; Nucleophilic substitution

Indexed keywords


EID: 79957524574     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2011.32.5.1741     Document Type: Article
Times cited : (2)

References (13)
  • 3
    • 79957438113 scopus 로고    scopus 로고
    • and references therein
    • Park, Y. S. Tetrahedron: Asymmetry 2009, 43, 8253, and references therein.
    • (2009) Tetrahedron: Asymmetry , vol.43 , pp. 8253
    • Park, Y.S.1
  • 4
    • 18944373681 scopus 로고    scopus 로고
    • The absolute configurations of (R)-3 and (R)-15-18 were determined by comparison of CSP-HPLC retention time with the reported values
    • The absolute configurations of (R)-3 and (R)-15-18 were determined by comparison of CSP-HPLC retention time with the reported values. (a) Kim, H. J.; Shin, E.-K.; Chang, J.-Y.; Kim, Y.; Park, Y. S. Tetrahedron Lett. 2005, 46, 4115.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 4115
    • Kim, H.J.1    Shin, E.-K.2    Chang, J.-Y.3    Kim, Y.4    Park, Y.S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.