Dibenzoate chirality rule

Alternatively, the absolute configuration of dihydrodiol derivatives of arenes can be established by the application of the dibenzoate chirality rule to the bis(4-dimethyloaminobenzoate) or bis(4-dimethylaminocinnamate) derivative (Section 4.4.2.4.1.). 

The dibenzoate chirality rule 155, 156 extends the application of the exciton chirality method to molecules containing no suitable chromophore, but, rather two hydroxy groups which can be converted to benzoates or cinnamates. For example, the dibenzoate 1, obtained by benzoy-lation of the ra-diol, from microbial oxidation of ethylbenzene, displays a negative exciton Cotton effect and is hence assigned the 1 S.2R configuration157. 

The amplitude (A) of the exciton Cotton effect is inversely proportional to the square of the interchromophoric distance. Thus, weak exciton split Cotton effects are expected for remote dibenzoates. Nevertheless, exciton Cotton effects were used for the assignment of the configuration of dibenzoates in a steroidal skeleton separated by as many as seven or eight C—C bonds158. In one application, the absolute configuration of Wieland-Miescher ketone (—)-2 was established by the use of the dibenzoate chirality rule for the 4-bromobenzoylated derivatives of the epimeric 1,5-diols 3 and 4, obtained by reduction of (-)-2159. 

The absolute configurations of two rigid cyclic diols, (—)-adamantane-2,6-diol and ( )-spiro[5.5]undecane-3,9-diol, have been determined by the application of the dibenzoate chirality rule to the bis(p-methoxybenzoate) derivatives195,196. 

Due to the complexity of conformational equilibria, the application of the dibenzoate chirality rule to determination of the absolute configuration of acyclic diols and polyols requires cautious evaluation of the CD data. For example, (0,0)-dibenzoyl derivatives of diesters and N.N.N ,AT-tetraalkyldiamides of (/t,f )-tartaric acid give exciton Cotton effects of opposite sign due to the preference of diesters for a planar and tetraalkyldiamides for a gauche conformation of the carbon chain176. 

The dibenzoate chirality rule 153,156 (Section 4.4.2.4.1.) allows determination of the absolute configuration of dibenzoylated amino alcohols186 187 198, mercapto alcohols188 and diamines187. For acyclic /1-amino alcohol O.A-dibcnzoate derivatives the dominant rotatory... 

The signs of the first and second Cotton effects in complexes with diols are opposite to those determined by the classical dibenzoate chirality rule (compare Figure 26).263 This means that the chiral guest induces an opposite chirality in the resorcarene host 129. Thus, 129 can be used as a supramolecular CD probe for the assignment of the absolute configurations of glycols and alcohols. 

To determine the absolute configuration of optically active organic compounds, there are two nonempirical methods. One is the Bijvoet method in the X-ray crystallographic structure analysis, which is based on the anomalous dispersion effect of heavy atoms. - The X-ray Bijvoet method has been extensively applied to various chiral organic compounds since Bijvoet first succeeded in determination of the absolute stereochemistry of tartaric acid in 1951. The second method is a newer one based on the circular dichroism (CD) spectroscopy. Harada and Nakanishi have developed the CD dibenzoate chirality rule, a powerful method for determination of the absolute configuration of glycols, which was later generalized as the CD exciton chirality method. 8 The absolute stereochemistry of various natural products has been determined by application of this nonempirical method. 

The well-established dibenzoate chirality rule (Harada and Nakanishi, 1969a,b, 1972) has been extended to Af,iV -dibenzoyldiamino acids (22). The... 

The application of CD exciton coupling formalism to structural analysis started as the dibenzoate chirality rule , which became the exciton chirality method when it was expanded to include the coupling between a variety of chromophores for determining the absolute configurations and/or... 

The absolute configuration of (-)-spiro[4.4]nonane-l,6-dione was determined by application of Horeau s method of optical rotations.[45] In support of the assignment, and with greater certainty, the Exciton Chirality Rule was applied to the bis-p-dimethylamino-benzoate of the cis,trans-diol obtained following reduction of the diketone. The cis,trans-diol is readily distinguished by NMR from the C2-symmetry cis,cis and rrans,rrans-diols. Since the cis,trans-diol dibenzoate from the (-)-dione exhibits a (-) exciton chirality CD, it follows that the absolute configuration of the dione is that shown in Figure 37. The absolute stereochemistry is easily determined by CD. 

To determine the ACs of acyclic 1,2-glycols, the CD exciton chirality method has been applied to their dibenzoates or bis(2-anthroates), which show typical bisignate Cotton effects (see Section 9.04.4) as exemplified in Figures 27 and 28.72,73 Acyclic dibenzoates or bis(2-anthroates) can rotate around the bond connecting two benzoate or 2-anthroate chromophores, and therefore the CD sign depends on the conformational equilibrium. From the data of many examples, general rules were derived as shown in Figures 27 and 28. 

Nakanishi s method is based on the splitting of CD waves when two chromopho-res on a chiral molecule are close in space (the dibenzoate rule). Such is the case with dibromobenzoates of sugars which have a 1,2 or 1,3 relationship. In the first version of the method, saponins were permethylated, methanolyzed with acid and the liberated OH positions were p-bromobenzoylated (44). As terminal sugars are fully methylated and UV transparent, they need not be considered. Branched sugars (two substitutions at least) 3deld di-or tri-benzoates with exciton-split CD curves. The difference in Ae values of the two extrema of split CD curves is directly related to the respective positions of the benzoates (1, 2 eq-eq = 1, 2 eq-ax = 62 1, 2 ax-ax = 6 1, 3 eq-eq = 0 1, 3 eq-ax = 16). The sensitivity of circular dichroism makes the method suitable for microassays. Typical analyses are performed on a 100 pg scale (nanomolar levels). 

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