1980
DOI: 10.1080/00021369.1980.10864411
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Structures and Syntheses of Two Phenolic Amides fromPiper nigrumL.

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Cited by 18 publications
(6 citation statements)
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“…The HRESIMS spectrum showed a deprotonated molecule of m / z 403.1380 (calcd for 403.1393), corresponding to a molecular formula of C 21 H 24 O 8 containing 10 degrees of unsaturation. The 1 H and 13 C NMR spectral data of 1 were found to be similar to those of p -hydroxyphenethyl trans -ferulate ( 5 ), which in turn was identified by comparison of its NMR data with literature data. ,, A fragment ion of m / z 193 in the CID product ion spectrum suggested the presence of a feruloyl unit. , The 1 H NMR spectrum of 1 displayed signals at δ 7.588 (1H, d, J = 16.0 Hz) and 6.322 (1H, d, J = 16.0 Hz), indicating the presence of two trans -coupled olefinic protons, and signals at δ 3.929 (3H, s), 3.889 (3H, s), and 3.278 (3H, s) attributable to three methoxyl groups. In addition, two sets of 1,3,4-trisubstituted phenyl units (ABX system) were revealed by signals at δ 7.061 (1H, dd, J = 8.2, 2.0 Hz), 7.030 (1H, d, J = 2.0 Hz), 6.915 (1H, d, J = 8.2 Hz), 6.905 (1H, d, J = 8.6 Hz), 6.810 (1H, d, J = 2.0 Hz), and 6.806 (1H, dd, J = 8.6, 2.0 Hz) and confirmed by the COSY spectrum.…”
Section: Resultsmentioning
confidence: 69%
“…The HRESIMS spectrum showed a deprotonated molecule of m / z 403.1380 (calcd for 403.1393), corresponding to a molecular formula of C 21 H 24 O 8 containing 10 degrees of unsaturation. The 1 H and 13 C NMR spectral data of 1 were found to be similar to those of p -hydroxyphenethyl trans -ferulate ( 5 ), which in turn was identified by comparison of its NMR data with literature data. ,, A fragment ion of m / z 193 in the CID product ion spectrum suggested the presence of a feruloyl unit. , The 1 H NMR spectrum of 1 displayed signals at δ 7.588 (1H, d, J = 16.0 Hz) and 6.322 (1H, d, J = 16.0 Hz), indicating the presence of two trans -coupled olefinic protons, and signals at δ 3.929 (3H, s), 3.889 (3H, s), and 3.278 (3H, s) attributable to three methoxyl groups. In addition, two sets of 1,3,4-trisubstituted phenyl units (ABX system) were revealed by signals at δ 7.061 (1H, dd, J = 8.2, 2.0 Hz), 7.030 (1H, d, J = 2.0 Hz), 6.915 (1H, d, J = 8.2 Hz), 6.905 (1H, d, J = 8.6 Hz), 6.810 (1H, d, J = 2.0 Hz), and 6.806 (1H, dd, J = 8.6, 2.0 Hz) and confirmed by the COSY spectrum.…”
Section: Resultsmentioning
confidence: 69%
“…The methylene chloride extract of the fruits of white pepper was separated in the same way described previously. 6 (64), 72 (4), 57 (16), 43 (10). These data were identical with those of synthetic pellitorine and the mixed melting point showedno depression.…”
mentioning
confidence: 99%
“…Identification of known compounds was done on the basis of the spectroscopic data and comparisons with those found in the literature as achilleamide ( 1 ), 2,4-( E , E )-dodecadienyl piperidide ( 2 ), 1-cinnamoylpiperidine ( 4 ), N - trans -feruloyl piperidine ( 5 ), coumaperine ( 6 ), piperanine ( 7 ), piperoleine A ( 8 ), piperoleine B ( 9 ), piperine ( 11 ), pipernonaline ( 12 ), piperchabamide B ( 13 ), piperchabamide C ( 14 ), piperettine ( 15 ), dehydropipernonaline ( 16 ), (2 E ,4 E ,12 E )-13-(3,4-methylenedioxyphenyl)-1-(1-piperidinyl)-2,4,12-tridecatrien-1-one ( 17 ), tricholeine ( 18 ), piperyline ( 19 ), brachyamide B ( 20 ), 1-[(2 E ,10 E )-11-(3,4-methylenedioxyphenyl)-2,10-undecenoyl]­pyrrolidine ( 21 ), piperettyline ( 22 ), 6,7-dehydrobrachyamide B ( 23 ), 1-[(2 E ,4 E ,10 E )-11-(3,4-methylenedioxyphenyl)-2,4,10-undecatrienoyl]­pyrrolidine ( 24 ), brachyamide A ( 25 ), pellitorine ( 26 ), kalecide ( 27 ), N -isobutyl-(2 E ,4 E )-hexadecadienamide ( 28 ), N -isobutyl-(2 E ,4 E )-octadecadienamide ( 29 ), N -isobutyl-(2 E ,4 E ,12 Z )-octadeca-2,4,12-trienamide ( 30 ), N -isobutyl-(2 E ,4 E ,14 Z )-eicosa-2,4,14-trienamide ( 31 ), piperlonguminine ( 32 ), piperchabamide D ( 33 ), retrofractamide A ( 34 ), retrofractamide B ( 35 ), guineensine ( 36 ), brachystamide B ( 37 ), feruloyltyramine ( 39 ), N - trans -feruloyldopamine ( 40 ), (2 E ,4 E )-5-(3,4-methylenedioxyphenyl)-2,4-pentadienal ( 45 ), piperic acid ( 46 ), methyl piperate ( 47 ), (+)-bornyl piperate ( 49 ), (6 E )-7-(3,4-methylenedioxyphenyl)-heptenoic acid ( 50 ), (8 E )-9-(3,4-methylenedioxyphenyl)-nonenoic acid ( 51 ), cubebinol ( 52 ), (−)-dehydrodiconiferyl alcohol ( 53 ), (−)-secoisolariciresinol ( 54 ), and (2 R ,3 R )-2-[(3,4-dimethoxyphenyl)­methyl]-3-[(3,4,5-trimethoxyphenyl)­methyl]-1,4-butanediol ( 55 ) …”
Section: Resultsmentioning
confidence: 99%