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Volumn 56, Issue 3, 2013, Pages 307-311

First way of enantioselective synthesis of moxifloxacin intermediate

Author keywords

(S, S) 2; 8 diazobicyclo 4.3.0 nonane; enantioselective synthesis; moxifloxacin intermediate

Indexed keywords

(S, S)-2; 8-DIAZOBICYCLO [4.3.0] NONANE; CHIRAL INDUCTION; ENANTIOSELECTIVE SYNTHESIS; MOXIFLOXACIN; PURIFICATION METHOD; SYNTHETIC PROCESS; TOTAL YIELD;

EID: 84879689185     PISSN: 16747291     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11426-012-4803-7     Document Type: Conference Paper
Times cited : (13)

References (16)
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  • 13
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    • Euromediator analogs: Synthesis of cis (2R, 3S) and trans (2S, 3S)-2, 3-piperidine dicarboxylic acids from (2S)-2-phenylglycinol
    • 10.1016/0040-4039(95)00088-T 1:CAS:528:DyaK2MXktl2ru7o%3D
    • Agami C, Kadouri-Puchot C, Le Guen V, Vaissermann J. Neuromediator analogs: Synthesis of cis (2R, 3S) and trans (2S, 3S)-2, 3-piperidine dicarboxylic acids from (2S)-2-phenylglycinol. Tetrahedron Lett, 1995, 36: 1657-1660
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  • 15
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    • Synthese asymetrique de l'acide aspartique optiquement pur
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    • Formation of 1, 2, 3, 4-tetrahydro-2-pyridones by aza-annulation of imines with acrylate derivatives
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.