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Volumn 75, Issue 17, 2010, Pages 6012-6015

Practical enantiospecific synthesis of an orthogonally protected 1,4- trans -1,5- cis - 4,5-diamino-2-cyclopenten-1-ol derivative

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTENES; DIAMINE MOIETIES; ENANTIOSPECIFIC SYNTHESIS; OVERMAN REARRANGEMENT;

EID: 77956148101     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1009118     Document Type: Article
Times cited : (11)

References (43)
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  • 25
    • 77953299014 scopus 로고    scopus 로고
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    • Precedences of diastereoconvergent additions to t -BS imines are very rare
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    • McMahon, J.P.1    Ellman, J.A.2
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    • Analogous N -Ts-imines were unstable, while N -benzylimines gave lower (35-84%) yields:;;, In contrast to t -BS imines, the drs for p -toluenesulfinylimines were controlled by the sulfur chirality:;; Org. Lett. 2008, 2179
    • Analogous N -Ts-imines were unstable, while N -benzylimines gave lower (35-84%) yields: Cossy, J.; Pévet, I.; Meyer, C. Eur. J. Org. Chem. 2001, 2841 In contrast to t -BS imines, the drs for p -toluenesulfinylimines were controlled by the sulfur chirality: Zhou, D.; Staake, M.; Patterson, S. E. Org. Lett. 2008, 10, 2179
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.