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Volumn 45, Issue 7, 2004, Pages 1481-1483

Synthesis of orthogonally protected 3,8-diazabicyclo[3.2.1]octane-2- carboxylic acid - A versatile building block for the synthesis of cocaine analogues

Author keywords

3,8 Diazabicyclo 3.2.1 octane; Building block; Cocaine analogue; Orthogonal amine protection groups

Indexed keywords

3,8 DIAZABICYCLO[3.2.1]OCTANE 2 CARBOXYLIC ACID; ALPHA AMINO ACID; BETA AMINO ACID; CARBOXYLIC ACID DERIVATIVE; COCAINE DERIVATIVE; PYROGLUTAMIC ACID; UNCLASSIFIED DRUG;

EID: 1642497613     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.12.031     Document Type: Article
Times cited : (5)

References (38)
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    • For a racemic synthesis of the 3,8-diazabicyclo[3.2.1]octane skeleton, see:
    • For a racemic synthesis of the 3,8-diazabicyclo[3.2.1]octane skeleton, see: Schipper E., Boehme W.R. J. Org. Chem. 26:1961;3599-3602.
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    • For an asymmetric synthesis of a corresponding 3,8-diazabicyclo[3.2.1] octan-2-one, see:
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    • note
    • 3: C, 52.17; H, 6.57; N, 15.21. Found C, 52.10; H, 6.41; N, 15.17.
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    • note
    • 6: C, 56.46; H, 7.11; N, 8.23. Found C, 56.39; H, 7.04; N, 8.34.
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    • I . CCDC-187193 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44-1223-336033; e-mail: deposit@ccdc.cam.ac.uk ).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.