1. Chirality, 2008, Volume 20 Issue 5, Pages 691 - 723
Nobuyuki Harada
Determination of absolute configurations by X-ray crystallography and 1H NMR anisotropy
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http://dx.doi.org/10.1002/chir.20478Helmut Duddeck, Edison Díaz Gómez
Chiral recognition of ethers by NMR spectroscopy
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http://dx.doi.org/10.1002/chir.20605Chuan-Qing Kang, Hai-Quan Guo, Xue-Peng Qiu, Xiao-Li Bai, Hai-Bo Yao, Lian-Xun Gao
Assignment of absolute configuration of cyclic secondary amines by NMR techniques using Mosher's method: a general procedure exemplified with (-)-isoanabasine
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http://dx.doi.org/10.1002/mrc.1716Jinhai Gao, Hansjoerg Haas, Kate Yaping Wang, Zhuoliang Chen, Werner Breitenstein, Srinivasan Rajan
The use of MPA amide for the assignment of absolute configuration of a sterically hindered cyclic secondary amine by mix and shake NMR method
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http://dx.doi.org/10.1002/mrc.2115William Adcock, Anil N. Abeywickrema, V. Sankar Iyer, Gaik B. Kok
Transmission of polar substituent effects through the bicyclo[2.2.2]octane ring system as monitored by NMR shifts: A 13C NMR study of 4-substituted-1-methylbicyclo[2.2.2]octanes
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http://dx.doi.org/10.1002/mrc.1260240306Ryszard Gawinecki, Erkki Kolehmainen, Zdzislaw Kucybala, Borys Omialowski, Reijo Kauppinen.
Predominance of resonance over polar effects on 1H, 13C and 15N NMR substituent chemical shifts in N-arylglycines
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http://dx.doi.org/10.1002/(SICI)1097-458X(1998110)36:11<848::AID-OMR379>3.0.CO;2-O