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Volumn 14, Issue 22, 2003, Pages 3447-3453

An efficient enantioselective synthesis of an indane acetic acid derivative: Methyl (2S)-2-[(1S)-5-hydroxy-2,3-dihydro-1H-inden-1-yl]butanoate

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID DERIVATIVE; INDAN DERIVATIVE; INDENE DERIVATIVE; METHYL 2,5 HYDROXY 2,3 DIHYDRO 1H INDEN 1 YLBUTANOIC ACID; UNCLASSIFIED DRUG;

EID: 0242710856     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2003.07.021     Document Type: Article
Times cited : (13)

References (24)
  • 14
    • 84855209169 scopus 로고
    • For a recent review on Reformatsky reaction, see:
    • For a recent review on Reformatsky reaction, see: Furstner A. Synthesis. 1989;571.
    • (1989) Synthesis , pp. 571
    • Furstner, A.1
  • 18
    • 84889342346 scopus 로고    scopus 로고
    • Chichester: John Wiley & Sons Ltd. and references cited therein
    • Laue T., Plagens A. Named Organic Reactions. 1998;224 John Wiley & Sons Ltd, Chichester. and references cited therein.
    • (1998) Named Organic Reactions , pp. 224
    • Laue, T.1    Plagens, A.2
  • 22
    • 85030951150 scopus 로고    scopus 로고
    • The ee was determined by chiral HPLC under the following conditions: 5% isopropanol/95% hexanes, each containing 0.1% TFA; 1.5 ml/min flow rate; 284 nm UV detection.
    • The ee was determined by chiral HPLC under the following conditions: 5% isopropanol/95% hexanes, each containing 0.1% TFA; 1.5 ml/min flow rate; 284 nm UV detection.
  • 23
    • 85030942557 scopus 로고    scopus 로고
    • 1H NMR nor chiral HPLC.
    • 1H NMR nor chiral HPLC.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.