Tuning mechanism in a two-component columnar host system composed of 1,2-diphenylethylenediamine and 1,1′-binaphthyl-2,2′-dicarboxylic acid

Organic Letters

Volumn 10, Issue 3, 2008, Pages 469-471

  Imai, Yoshitane ^a   Kawaguchi, Kakuhiro ^a   Murata, Katuzo ^a   Sato, Tomohiro ^b   Kuroda, Reiko ^b,c   Matsubara, Yoshio ^a  

^a KINKI UNIVERSITY   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^c UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1,1' BINAPHTHYL 2,2' DICARBOXYLIC ACID; 1,1'-BINAPHTHYL-2,2'-DICARBOXYLIC ACID; 1,2 DIANILINOETHANE; 1,2-DIANILINOETHANE; DICARBOXYLIC ACID; ETHYLENEDIAMINE DERIVATIVE; NAPHTHALENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; STEREOISOMERISM; X RAY CRYSTALLOGRAPHY;

CRYSTALLOGRAPHY, X-RAY; DICARBOXYLIC ACIDS; ETHYLENEDIAMINES; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; NAPHTHALENES; STEREOISOMERISM;

EID: 39049096876     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol7028433     Document Type: Article

References (24)

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18. A mixture of (1R,2R)-1 (5 mg, 0.024 mmol), (1S,2S)-1 (5 mg, 0.024 mmol), (R)-2 (8 mg, 0.024 mmol), and (S)-2 (8 mg, 0.024 mmol) was dissolved in n-HexOH or EtOH (2 mL) and left to stand at room temperature. After a few days, several colorless crystals were produced.
19. This weight is the total crop of obtained crystals in one batch.
20. This weight is the total crop of obtained chiral crystals in one batch.
21. 2) = 0.0831 using 5289 reflections with I > 2.0σ(I), R(all data) = 0.1319, T= 120(2) K; CCDC 652860.
22. 2) = 0.0671 using 4689 reflections with I > 2.0σ(I), R(all data) = 0.1169, T = 120(2) K; CCDC 668015. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/ retrieving.html (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB21EZ, UK; fax: (+44)1223-336-033; deposit@ccdc.cam.ac.uk).
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