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Volumn 76, Issue 1, 2011, Pages 234-244

Asymmetric synthesis of chiral N-sulfinyl 3-alkyl- and 3-arylpiperidines by α-alkylation of N-sulfinyl imidates with 1-chloro-3-iodopropane

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC SYNTHESIS; DIASTEREOMERIC RATIOS; GOOD YIELD; IMIDATES; SUBSEQUENT REDUCTION;

EID: 78650861483     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1020807     Document Type: Article
Times cited : (38)

References (88)
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    • For the synthesis of chiral 2-substituted N -sulfinyl piperidines, see
    • For the synthesis of chiral 2-substituted N -sulfinyl piperidines, see: Reddy, L. R.; Das, S. G.; Liu, Y.; Prashad, M. J. Org. Chem. 2010, 75, 2236
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    • It is speculated that the nature of the α-substituent of the imidates influences the E/Z-ratio of the lithium enolates and determines the diastereomeric ratio of the reaction products.
    • It is speculated that the nature of the α-substituent of the imidates influences the E/Z-ratio of the lithium enolates and determines the diastereomeric ratio of the reaction products.
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    • PCT Int. Appl., WO 2007126362 A1 20071108.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.