메뉴 건너뛰기




Volumn 47, Issue 8, 2006, Pages 1337-1340

Remote asymmetric trifluoromethylation induced by chiral sulfinyl group: Synthesis of enantiomerically pure 1-(2-naphthyl)-2,2,2-trifluoroethanol

Author keywords

1,4 Asymmetric induction; Chiral alcohol; Sulfinyl group; Trifluoromethylation

Indexed keywords

(TRIFLUOROMETHYL)TRIMETHYLSILANE; 1 (2 NAPHTHYL) 2,2,2 TRIFLUOROETHANOL; 1 [(2,4,6 TRIISOPROPYLPHENYL)SULFINYL] 2 NAPHTHALDEHYDE; ALDEHYDE DERIVATIVE; FLUORIDE; SILANE DERIVATIVE; TETRAMETHYLAMMONIUM FLUORIDE; TRIFLUOROETHANOL; UNCLASSIFIED DRUG;

EID: 30944459019     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.12.061     Document Type: Article
Times cited : (31)

References (29)
  • 12
    • 0033585063 scopus 로고    scopus 로고
    • For other enantioselective trifluoromethylation, see: Y. Kuroki, and K. Iseki Tetrahedron Lett. 40 1999 8231 8234
    • (1999) Tetrahedron Lett. , vol.40 , pp. 8231-8234
    • Kuroki, Y.1    Iseki, K.2
  • 26
    • 30944433483 scopus 로고    scopus 로고
    • note
    • 4, and concentrated under reduced pressure to leave a residue, which was purified by column chromatography (silica gel 10 g, hexane/ethyl acetate = 95/5) to give 2c (77.5 mg, 85%).
  • 27
    • 30944446071 scopus 로고    scopus 로고
    • note
    • R, 12.1 (R), 17.2 (S) min.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.