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Volumn 27, Issue 12, 2006, Pages 2019-2022

Enantioselective synthesis of cyclic amino alcohols: Cis-1-amino-2-indanol

Author keywords

Absolute stereocontrol; cis 1 Amino 2 indanol; Enantioselective synthesis

Indexed keywords

ALCOHOLS; AMINES; CYCLIC VOLTAMMETRY; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 33845787409     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2006.27.12.2019     Document Type: Article
Times cited : (8)

References (19)
  • 10
    • 0003412412 scopus 로고    scopus 로고
    • Wiley-Interscience: New York
    • th ed; Wiley-Interscience: New York, 2001; p 166.
    • (2001) th Ed , pp. 166
  • 11
    • 33845723871 scopus 로고    scopus 로고
    • note
    • (a) The notation syn/anti is reversed going from a cyclic to an acyclic backbone as these terms are dependent on how the "main chains" are drawn. The notation lk/ul, normally the most unambiguous method to describe a relative stereochemistry, would not have been so clear-cut in this case as the notation is based on the CIP system, therefore changes depending on substituent X (see Schemes 1 and 2).
  • 15
    • 33845786772 scopus 로고    scopus 로고
    • note
    • 2- signals only after the oxazolidinone formation, suggesting a conformational restriction caused by the 5-membered ring. Indeed, the subsequent cyclization (an intramolecular Friedel-Crafts acylation) was unsuccessful when there was no conformational restriction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.