메뉴 건너뛰기




Volumn 73, Issue 24, 2008, Pages 9771-9774

Short enantioselective syntheses of trans-5-alkylprolines from new functionalized amino alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ACIDIC MEDIUMS; AMINO ALCOHOLS; BICYCLIC COMPOUNDS; CHEMICAL EQUATIONS; ENANTIOPURE; ENANTIOSELECTIVE SYNTHESES; ENOL ETHERS; FUNCTIONALIZED;

EID: 58049195781     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8014243     Document Type: Article
Times cited : (12)

References (63)
  • 2
    • 38949165216 scopus 로고    scopus 로고
    • For some selected examples, see: b
    • For some selected examples, see: (b) Halab, L.; Gosselin, F.; Lubell, W. D. Biopolymers 2000, 55, 101-122.
    • (2000) Biopolymers , vol.55 , pp. 101-122
    • Halab, L.1    Gosselin, F.2    Lubell, W.D.3
  • 7
    • 0037043180 scopus 로고    scopus 로고
    • For some selected reviews, see: a
    • For some selected reviews, see: (a) List, B. Tetrahedron 2002, 58, 5573-5590.
    • (2002) Tetrahedron , vol.58 , pp. 5573-5590
    • List, B.1
  • 10
  • 11
    • 34250371777 scopus 로고    scopus 로고
    • For some selected recent examples of proline organocatalysis, see: a
    • For some selected recent examples of proline organocatalysis, see: (a) Rodríguez, B.; Bruckmann, A.; Bolm, C. Chem. - Eur. J. 2007, 13, 4710-4722.
    • (2007) Chem. - Eur. J , vol.13 , pp. 4710-4722
    • Rodríguez, B.1    Bruckmann, A.2    Bolm, C.3
  • 31
    • 0026553743 scopus 로고
    • For the synthesis of 5-alkyl proline derivatives, see: a
    • For the synthesis of 5-alkyl proline derivatives, see: (a) Manfré, F.; Kern, J.-M.; Biellmann, J.-F. J. Org. Chem. 1992, 57, 2060-2065.
    • (1992) J. Org. Chem , vol.57 , pp. 2060-2065
    • Manfré, F.1    Kern, J.-M.2    Biellmann, J.-F.3
  • 52
    • 0001203714 scopus 로고    scopus 로고
    • For the synthesis of 2,5-pyrrolidines by opening bicyclic oxazolidines, see also: (a) Huang, P. Q.; Arsenyadis, S.; Husson, H.-P. Tetrahedron Lett. 1987, 28, 547-550.
    • For the synthesis of 2,5-pyrrolidines by opening bicyclic oxazolidines, see also: (a) Huang, P. Q.; Arsenyadis, S.; Husson, H.-P. Tetrahedron Lett. 1987, 28, 547-550.
  • 55
    • 58049205937 scopus 로고    scopus 로고
    • D with those reported in the literature
    • D with those reported in the literature: ref 10.
  • 62
    • 58049194820 scopus 로고    scopus 로고
    • Atomic coordinates, bond lengths and angles, and thermal parameters of compound 7a have been deposited at the Cambridge Crystallographical Data Center with the deposition number CCDC 661332.
    • Atomic coordinates, bond lengths and angles, and thermal parameters of compound 7a have been deposited at the Cambridge Crystallographical Data Center with the deposition number CCDC 661332.
  • 63
    • 58049205936 scopus 로고    scopus 로고
    • The trans stereochemistry of the proline derivatives was ascertained on the basis of the NMR analysis: the 1H NMR spectra of compounds 1a-b showed an apparent triplet for the α proton, a feature for the trans diastereoisomer see ref 6c
    • 1H NMR spectra of compounds 1a-b showed an apparent triplet for the α proton, a feature for the trans diastereoisomer (see ref 6c).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.