Spectroscopy heteronuclear multiple-bond

C.E. Hadden, G.E. Martin, V.V. Krishnamurthy, Constant time inverse-detection gradient accordion rescaled spectroscopy heteronuclear multiple bond correlation— CIGAR-HMBC, Magn. Reson. Chem. 38 (2000) 143-147. 

Because of the complexity of the polyether antibiotics tittle progress has been made in stmcture determination by the chemical degradation route. X-ray methods were the techniques most successfully applied for the early stmcture elucidations. Monensin, X206, lasalocid, lysocellin, and salinomycin were included in nineteen distinct polyether x-ray analyses reported in 1983 (190). Use of mass spectrometry (191), and H (192) and nmr (141) are also reviewed. More recently, innovative developments in these latter techniques have resulted in increased applications for stmcture determinations. Eor example, heteronuclear multiple bond connectivity (hmbc) and homonuclear Hartmann-Hahn spectroscopy were used to solve the stmcture of portimicin (14) (193). East atom bombardment mass spectrometry was used in solving the stmctures of maduramicin alpha and co-factors (58). 

W. Schoefberger, J. Schlagnitweit and N. Muller, Recent Developments in Heteronuclear Multiple-Bond Correlation Experiments, in Annual Reports on NMR Spectroscopy, G. A. Webb (ed.), Vol. 72, Academic Press, 2011, pp. 1-60. 

In the case of the 7-hydroxy-substituted compounds 44 (Scheme 2), 54 different derivatives were investigated by 13C NMR spectroscopy and, in some cases, also by 1SN NMR spectroscopy <1995JST(335)273>. With the help of proton-coupled 13C NMR spectra, semi-selective INEPT (insensitive nuclei enhanced by polarization transfer) experiments, and heteronuclear multiple bond correlation (HMBC) two-dimensional 2D-NMR spectra, all shifts could be unequivocally assigned. While the C-7 shifts did not allow the existing tautomeric situation to be determined, a clear decision could be made by H NMR spectroscopy in this respect. The 1SN NMR spectra revealed an equilibrium between the N(4)H and N(3)H tautomeric forms, which is fast on the NMR timescale. 

In order to assign the chemical shifts of the carbon atoms of the conjugated diene system of each CLA isomer, it was necessary to conduct INADEQUATE, HMBC (heteronuclear multiple bond correlation) and two-dimensional 1H-13C correlation spectroscopy (COSY) techniques on the carbon signals of the diene system of the ,Z-isomers. The results of these experiments for the CLA isomers are summarized in Table 13. 

HMBC Heteronuclear multiple-bond correlation spectroscopy To elucidate structure of organic molecules To establish long-range (i.e., multibond) heteronuclear coupling... 

Hadden, C.E., Martin, G.E., and Krishnamurthy, V.V., Improved performance accordion heteronuclear multiple-bond correlation spectroscopy — IMPEACH-MBC, J. Magn. Reson., 140, 274, 1999. 

Notably, two isomeric products can be generated. The usual infrared (IR) and mass spectra as well as H and 13C NMR chemical shifts could not define which isomer was formed. The authors used different NMR techniques, such as 2-D heteronuclear multiple bond correlation (HMBC) experiments and phase-sensitive nuclear overhauser enhancement spectroscopy (NOESY) measurements to elucidate the product s structure. 

The fatty acyl substituents were mainly of three types saturated straight-chain C,6-C,9 acids C21-C25 mycosanoic acids and C24-C28 mycolipanolic acids. Analysis of one of the major 2,3-di-O-acyltrehaloses by two-dimensional H-chemical-shift-correlated and H-detected heteronuclear multiple-bond correlation spectroscopy established that the C18 saturated straight-chain acyl group was located at the 0-2 position and that the C24 mycosanoyl substituent was at the 0-3 position of the same nonglycosylated terminus (structure 8). At least six molecular... 

Other strategies that show great promise in reducing NMR acquisition time utilise methods to obtain multiple sets of data from one experiment through a concept known as time-shared evolution. An example of this process that should find utility in natural products elucidation was demonstrated by a pulse sequence called CN-HMBC.93 Traditionally, a separate 13C-HMBC and 15N-HMBC were acquired independently. However, the CN-HMBC allows both 13C- and 15N-HMBC spectra to be obtained simultaneously. By acquiring both data sets simultaneously, an effective 50% time reduction can be achieved.93 This approach has also been demonstrated for a sensitivity-enhanced 2D HSQC-TOCSY (heteronuclear multiple bond correlation total correlation spectroscopy) and HSQMBC (heteronuclear single quantum... 

The structural connectivity derived from examination of the 111, 13C/DEPT, DQF-COSY, HMQC, and HMBC data (DEPT = distortionless enhancement by polarization transfer DQF = double quantum filtering COSY = correlation spectroscopy HMQC = heteronuclear multiple quantum correlation HMBC = heteronuclear multiple bond correlation) resulted in global reevaluation of sclerophytin B structure and demonstrated that this compound and the related alcohol are not composed of two ether bridges as in the originally formulated structure 37, but share the structural features depicted as 38 <20000L1879>. Comparison of 13C and 111 NMR data of Norte s... 

Two-dimensional NMR spectroscopy ((double quantum fdtering (DQF), correlation spectroscopy (COSY), hetero-nuclear multiple quantum correlation (HMQC), heteronuclear multiple bond correlation (HMBC)) as well as liquid secondary ionization mass spectrometry (LSI MS) and UV-Vis spectroscopies were used to establish crown structures of TTFs 33 ( =l-3). In the case of the macrocycle 33 ( = 1), two protons of each methylene group of the SCH2CH2O fragments were not identical and gave an AA BB system. This observation was in accordance with the expected low conformational mobility of the polyether bridge in ( )-33 ( = 1) as compared with (Z)-33 ( = 1). The macrocycle ( )-33 ( = 2) behaved similarly to ( )-33 ( =1), whereas the protons under discussion were equivalent in ( )-33 ( = 3) <2001CFJ447>. 

HMBC Heteronuclear Multiple Bond Correlation spectroscopy... 

For smaller quantities of compounds more sensitive inverse detected techniques are available, such as HMQC ( IH-I C one bond correlation via heteronuclear multiple quantum coherence, analogous to HETCOR) and HMBC (proton detected heteronuclear multiple bond correlation spectroscopy) (15). The last provide, in addition to the intraresidue multiple bond correlations, interresidue correlations between the anomeric carbon and the aglycone protons.We follow this general strategy for the structural determination of tri terpenoid saponins of Bupleurum fruticosum (16) andArdisia japonica (9). 

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