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Volumn 12, Issue 12, 2010, Pages 2822-2825

Stereochemical and skeletal diversity arising from amino propargylic alcohols

Author keywords

[No Author keywords available]

Indexed keywords

AMINOALCOHOL; FUSED HETEROCYCLIC RINGS;

EID: 77953592675     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol100914b     Document Type: Article
Times cited : (51)

References (34)
  • 5
    • 77953588678 scopus 로고    scopus 로고
    • For recent examples, see
    • For recent examples, see
  • 9
    • 77953592051 scopus 로고    scopus 로고
    • Experimental procedures to amide derivatives 2a,b are reported in Supporting Information
    • Experimental procedures to amide derivatives 2a,b are reported in Supporting Information.
  • 12
    • 77953597309 scopus 로고    scopus 로고
    • For examples, see
    • For examples, see
  • 18
    • 77953555060 scopus 로고    scopus 로고
    • Structures and stereochemistry of all the reported compounds were determined by detailed spectroscopic analysis, including X-ray structures of compounds 11a, 13a, and 14a (see Supporting Information)
    • Structures and stereochemistry of all the reported compounds were determined by detailed spectroscopic analysis, including X-ray structures of compounds 11a, 13a, and 14a (see Supporting Information).
  • 19
    • 77953569906 scopus 로고    scopus 로고
    • 1H NMR analysis of the inseparable mixture of the two regioisomers
    • 1H NMR analysis of the inseparable mixture of the two regioisomers.
  • 20
    • 77953554091 scopus 로고    scopus 로고
    • For the definition of endo / exo -mode selectivity in enyne RCM and recent examples, see
    • For the definition of endo / exo -mode selectivity in enyne RCM and recent examples, see
  • 24
    • 77953549847 scopus 로고    scopus 로고
    • Experimental reaction conditions to obtain skeletons 6 - 13b are reported in Supporting Information
    • Experimental reaction conditions to obtain skeletons 6 - 13b are reported in Supporting Information.
  • 33
    • 77953551497 scopus 로고    scopus 로고
    • Diverse selections were made from a larger collection using the "Diverse Molecules" component of Pipeline Pilot (Scitegic, Inc.) and the ECFP4 molecular fingerprints
    • Diverse selections were made from a larger collection using the "Diverse Molecules" component of Pipeline Pilot (Scitegic, Inc.) and the ECFP4 molecular fingerprints.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.