메뉴 건너뛰기




Volumn 13, Issue 6, 2002, Pages 559-562

Diastereoselective reduction of β-ketophosphonates derived from amino acids. A new entry to enantiopure β-hydroxy-γ-aminophosphonate derivatives

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; BORANE DERIVATIVE; CATECHOLBORANE; GAMMA AMINO BETA HYDROXYPHOSPHONATE; GAMMA N,N DIBENZYLAMINO BETA KETOPHOSPHONATE; PHOSPHONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037134288     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(02)00159-3     Document Type: Article
Times cited : (34)

References (24)
  • 18
    • 84992281805 scopus 로고    scopus 로고
    • 4 and evaporated under reduced pressure. The crude products were purified by flash chromatography
  • 19
    • 84992239962 scopus 로고    scopus 로고
    • 4 and evaporated under reduced pressure. The crude ketophosphonates were purified by flash chromatography
  • 20
    • 84992268398 scopus 로고    scopus 로고
    • High diastereoselectivity was also found in the reduction of β-amino-α-ketophosphonates with catecholborane in the presence of a catalytic amount of oxazaborolidine, see Ref. 3c
  • 21
    • 84992259447 scopus 로고    scopus 로고
    • 1H NMR at 400 MHz and purified by flash chromatography
  • 22
    • 84992233951 scopus 로고    scopus 로고
    • 31P NMR at 400 MHz
  • 23
    • 84992283762 scopus 로고    scopus 로고
    • Similar relations have been reported by related compounds, see Refs. 4a, b
  • 24
    • 84992241419 scopus 로고    scopus 로고
    • note


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.