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Methyl 1,2-(acetoxy-C,O)-3-hydroxy-5,6-dimethoxy-3-(3,4-dimethyloxyphenyl)indan-2-carboxylate

Sample Originator: Mark E. Light, Simon J. Coles, Michael B. Hursthouse, P. V. Subhash, S. G. A. Moinuddin, C. Kamakshi, R. Venkateswarlu, R. S. Ward and A. Pelter.

C23H24O9

InChI=1/C23H24O9/c1-27-16-7-6-12(8-17(16)28-2)22(26)14-10-19(30-4)18(29-3)9-13(14)15-11-20(24)32-23(15,22)21(25)31-5/h6-10,15,26H,11H2,1-5H3/t15-,22-,23+/m0/s1

Identification Number:10.5258/ecrystals/70
Controlled Keywords:cinnamates, coupling reactions, acidic-oxidative conditions, novel lignans
Date Created:02 April 2001
Deposited On:21 Jan 2008 15:28
Deposited By:A.N. Admin

Depositor Comments

It is confirmed that the dimerisation of methyl dialkoxycinnamates in acidic conditions yields trisubstituted indanes. When the reactions are carried out for 1.5 h/0°C in acidic conditions in the presence of DDQ then a variety of lignan types result, two of which represent new classes of lignans.DOI: 10.1016/S0040-4020(01)00742-6

Data collection parameters

Chemical formulaC23 H24 O9
Crystal morphology
Crystal systemOrthorhombic
Space group symbolPbca
Cell length a14.1493(4)
Cell length b17.3003(6)
Cell length c17.4340(7)
Cell angle alpha90.00
Cell angle beta90.00
Cell angle gamma90.00
Data collection temperature150(2)

Refinement results

Solution figure of merit
R Factor (Obs)0.0468
R Factor (All)0.0881
Weighted R Factor (Obs)0.1039
Weighted R Factor (All)0.1213

Citation: Light, Mark E. and Coles, Simon J. and Hursthouse, Michael B. and Subhash, P. V. and Moinuddin, S. G. A. and Kamakshi, C. and Venkateswarlu, R. and Ward, R. S. and Pelter, A. (2001) University of Southampton, Crystal Structure Report Archive. (doi:10.5258/ecrystals/70)
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Available Files

Final Result

01src400.CIF15k
01src400.cml8k

Validation

01src400_checkcif.htm8k

Refinement

01src400.RES8k
01src400_xl.lst43k

Solution

01src400.PRP5k

Processing

01src400.HKL795k

Other Files

01src400.mol4k
01src400_ellipsoid.gif21k

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