A new furanoeremophilane and a new eudesmane were isolated from the roots of Ligularia veitchiana. Their structures were elucidated as 1b, 10b-epoxy-6b-isobutyryloxy-9-oxo-furanoeremophilane and 8a-hydroxy-4 (15), 11...A new furanoeremophilane and a new eudesmane were isolated from the roots of Ligularia veitchiana. Their structures were elucidated as 1b, 10b-epoxy-6b-isobutyryloxy-9-oxo-furanoeremophilane and 8a-hydroxy-4 (15), 11-eudesmadiene by spectroscopic methods.展开更多
From Ligularia atroviolacea, four new eremophilendiolides, 81$-hydroxy-eremophil-3,7 (11)-dien-12,8α(14,6α)-diolide (1), 8β-methoxy-eremophil-3,7(11)-dien-12,8α(14,6α)-diolide (2), 8α-hydroxy-eremoph...From Ligularia atroviolacea, four new eremophilendiolides, 81$-hydroxy-eremophil-3,7 (11)-dien-12,8α(14,6α)-diolide (1), 8β-methoxy-eremophil-3,7(11)-dien-12,8α(14,6α)-diolide (2), 8α-hydroxy-eremophil-3,7(11)-dien-12,8lβ(14,6α)-diolide (3) and eremophil-3,7(11),8-trien-12,8 (14,6α)-diolide (4), as well as a known diolide (5) were isolated. Their structures were elucidated on the basis of 1D and 2D NMR as well as ESI-MS spectral data.展开更多
Chemical investigation of L. tongolensis afforded two new eremophilenolides, which were identified as 3β-(2'-methylbutanoyloxy)-8βH-eremophil-7(11)-en-12, 8α(14, 6α)-diolide (1)and 8βH-eremophil-3, 7(11...Chemical investigation of L. tongolensis afforded two new eremophilenolides, which were identified as 3β-(2'-methylbutanoyloxy)-8βH-eremophil-7(11)-en-12, 8α(14, 6α)-diolide (1)and 8βH-eremophil-3, 7(11)-dien-12, 8α (14, 6α)-diolide (2). Their structures were established by spectroscopic methods including 2D NMR experiments.展开更多
From the roots of Ligularia macrophylla, a bisesquiterpene, ligumacrophyllal was isolated and its structure was elucidated on the basis of spectroscopic methods.
A new eudesmanolide and a new aromatic derivative were isolated from the roots of Carpesium cernuun. Their structures were elucidated as 13-hydroxy-5,7(11)-eudesmadien-12,8-olide and 3-methyl-8-acetoxy-9,10-diisobuty...A new eudesmanolide and a new aromatic derivative were isolated from the roots of Carpesium cernuun. Their structures were elucidated as 13-hydroxy-5,7(11)-eudesmadien-12,8-olide and 3-methyl-8-acetoxy-9,10-diisobutyryloxy-p-cymene by spectral methods (EIMS, FAB-MS, 1D and 2D NMR).展开更多
Two new sesquiterpenes were isolated from the aerial parts of Inula japonica. Their structures were elucidated as 1-hydroxy-8-acetoxycostic acid methyl ester and 1-hydroxy-8-acetoxyisocostic acid methyl ester by spec...Two new sesquiterpenes were isolated from the aerial parts of Inula japonica. Their structures were elucidated as 1-hydroxy-8-acetoxycostic acid methyl ester and 1-hydroxy-8-acetoxyisocostic acid methyl ester by spectral methods.展开更多
A new isopropenyl benzofuran-type tetramer was isolated from the roots of ligularia stenocephala and its structure was established by spectroscopic methods.
From the roots of Sanguisorba alpina, a new triterpenoid was isolated and identified as 2-isobutyryloxy-19α, 25-dihydroxyursa-1, 12-dien-28-oic acid by means of spectral methods, named as aipinic acid.
Two new eremophilane sesquiterpenes, 15β-formic ether-6-oxo-furanoeremophilane (1) and 6α, 15β-epoxy eremophila-7(11)-en-8α, 12-olide (2) were isolation from the roots of Ligularia macrophylla. Their structu...Two new eremophilane sesquiterpenes, 15β-formic ether-6-oxo-furanoeremophilane (1) and 6α, 15β-epoxy eremophila-7(11)-en-8α, 12-olide (2) were isolation from the roots of Ligularia macrophylla. Their structures were deduced from spectroscopic methods and 2D NMR experiments.展开更多
Two new eremophilane sesquiterpenes 3β-angeloyloxy-8α-hydroxy-6β-methoxy eremophil-7 (11), 9 (10)-dien-8, 12-olide (1) and 3β-angeloyloxy-6β, 8α-dihydroxy-eremophi-7 (11), 9 (10)-dien-8, 12-olide (2) were isolat...Two new eremophilane sesquiterpenes 3β-angeloyloxy-8α-hydroxy-6β-methoxy eremophil-7 (11), 9 (10)-dien-8, 12-olide (1) and 3β-angeloyloxy-6β, 8α-dihydroxy-eremophi-7 (11), 9 (10)-dien-8, 12-olide (2) were isolated from Cacalia ainsliaeflora. Their structures were established by spectroscopic methods and 2D NMR experiments.展开更多
Two new minor steroidal saponins, (25R) spirostan-3β-ol-6-one-3-O-[α-L- arabinopyranosyl(1-4)]-β-D-glucopyranosidc (1) and (25S) spirost-5-en -3β, 17α, 27-triol-3-O- [α-L-arabinopyranosyl(1-6)]-β-D-glucopyranos...Two new minor steroidal saponins, (25R) spirostan-3β-ol-6-one-3-O-[α-L- arabinopyranosyl(1-4)]-β-D-glucopyranosidc (1) and (25S) spirost-5-en -3β, 17α, 27-triol-3-O- [α-L-arabinopyranosyl(1-6)]-β-D-glucopyranosidc (2) were isolated from the roots of Smilax lebrunii. Their structures were established on thc basis of chemical and spectral methods.展开更多
Chemical investigation of L.sagitta afforded two new cremophilenolides, which were identified as 6beta-angeloyloxy-10beta-hydroxy-8beta-methoxy-cremophil-7(11)-en-12, 8alpha-olide (1) and 6beta, 8beta-dimethoxy-10beta...Chemical investigation of L.sagitta afforded two new cremophilenolides, which were identified as 6beta-angeloyloxy-10beta-hydroxy-8beta-methoxy-cremophil-7(11)-en-12, 8alpha-olide (1) and 6beta, 8beta-dimethoxy-10beta-hydroxy-eremophil-7(11)-en-12, 8alpha-olide (2). Their structures were established by spectroscopic methods including 2D NMR experiments.展开更多
A new sesquiterpene and a new norsesquiterpene were isolated from the whole plant of Cacalia deltophylla (Maxim) Mattf. Their structures were elucidated as deltocacalone (1) and deltonorcacalol (2) by spectroscopic m...A new sesquiterpene and a new norsesquiterpene were isolated from the whole plant of Cacalia deltophylla (Maxim) Mattf. Their structures were elucidated as deltocacalone (1) and deltonorcacalol (2) by spectroscopic methods including 2D NMR.展开更多
A new sesquiterpene: 11,12,13-trihydroxy-4(15),7(8)-eudesmdien-9-one was isolated from Saussurea parviflora. The structure was elucidated on the basis of spectral evidence.
A new xanthanolide was isolated from the aerial parts of Carpesium longifolium. Its structure was elucidated as 1, 4-epoxy-5?hydroxy-10酘-xantha-11(13)-en-12, 8?olide by spectral methods (HRMS, 1D and 2D NMR).
Two new eremophilenolides (3b-angeloyloxy-8b, 10b-dihydroxy-6b-ethoxyeremophile- nolide (1) and 3b, 6b-diangeloyloxy-8a-methoxy-10a-hydroxyeremophilenolide (2) were isolated from the roots of Cacalia ainsliaeflora. T...Two new eremophilenolides (3b-angeloyloxy-8b, 10b-dihydroxy-6b-ethoxyeremophile- nolide (1) and 3b, 6b-diangeloyloxy-8a-methoxy-10a-hydroxyeremophilenolide (2) were isolated from the roots of Cacalia ainsliaeflora. Their structures were elucidated by spectroscopic methods.展开更多
A new eudesmanoilde was isolated from the aerial parts of Carpesium macrocephalum. Its structure was elucidated as 2?acetoxy-11酘-eudesma-4-en-12, 8?olide by spectral methods.
A New steroidal saponin was isolated from the rhizomes of Smilax lebrunii. On the basis of spectral and chemical methods, its structure was elucidated as:(25S)spirost-5-en-3β, 17α, 27-triol-3-0-[β-D-glucopyranosyl(...A New steroidal saponin was isolated from the rhizomes of Smilax lebrunii. On the basis of spectral and chemical methods, its structure was elucidated as:(25S)spirost-5-en-3β, 17α, 27-triol-3-0-[β-D-glucopyranosyl(1-4)][α-L-arabinopyranosyl(1-6)]-β-D-glucopyranoside.展开更多
Two minor steroidal saponins were isolated from the roots of Smilax menispermoidea.One of them is new and its structure was established as(25S) spirost-5-en-3β,17α,27-triol-3-O-[α-L-rhamnopyranosyl(1-4)]-β-D-gluco...Two minor steroidal saponins were isolated from the roots of Smilax menispermoidea.One of them is new and its structure was established as(25S) spirost-5-en-3β,17α,27-triol-3-O-[α-L-rhamnopyranosyl(1-4)]-β-D-gluco- pyranoside using spectroscopic and chemical methods.展开更多
基金supported by the National Natural Science Foundation of China(No.29972017)
文摘A new furanoeremophilane and a new eudesmane were isolated from the roots of Ligularia veitchiana. Their structures were elucidated as 1b, 10b-epoxy-6b-isobutyryloxy-9-oxo-furanoeremophilane and 8a-hydroxy-4 (15), 11-eudesmadiene by spectroscopic methods.
文摘From Ligularia atroviolacea, four new eremophilendiolides, 81$-hydroxy-eremophil-3,7 (11)-dien-12,8α(14,6α)-diolide (1), 8β-methoxy-eremophil-3,7(11)-dien-12,8α(14,6α)-diolide (2), 8α-hydroxy-eremophil-3,7(11)-dien-12,8lβ(14,6α)-diolide (3) and eremophil-3,7(11),8-trien-12,8 (14,6α)-diolide (4), as well as a known diolide (5) were isolated. Their structures were elucidated on the basis of 1D and 2D NMR as well as ESI-MS spectral data.
基金This work was supported by the NNSFC(No.20372029 and No,20021001)by the Key Project of Chinese Ministry of Education(No.104178).
文摘Chemical investigation of L. tongolensis afforded two new eremophilenolides, which were identified as 3β-(2'-methylbutanoyloxy)-8βH-eremophil-7(11)-en-12, 8α(14, 6α)-diolide (1)and 8βH-eremophil-3, 7(11)-dien-12, 8α (14, 6α)-diolide (2). Their structures were established by spectroscopic methods including 2D NMR experiments.
基金This work was supported by the NNSFC (No. 29972017).
文摘From the roots of Ligularia macrophylla, a bisesquiterpene, ligumacrophyllal was isolated and its structure was elucidated on the basis of spectroscopic methods.
基金This work was financially supported by the National Natural Science Foundation of China NO.29972017the Foundation of Ministry of Education of China for Doctoral Program NO.98073003National Key Basic Research Development Plan NO.G1998051113.
文摘A new eudesmanolide and a new aromatic derivative were isolated from the roots of Carpesium cernuun. Their structures were elucidated as 13-hydroxy-5,7(11)-eudesmadien-12,8-olide and 3-methyl-8-acetoxy-9,10-diisobutyryloxy-p-cymene by spectral methods (EIMS, FAB-MS, 1D and 2D NMR).
文摘Two new sesquiterpenes were isolated from the aerial parts of Inula japonica. Their structures were elucidated as 1-hydroxy-8-acetoxycostic acid methyl ester and 1-hydroxy-8-acetoxyisocostic acid methyl ester by spectral methods.
基金supoaed by the National Natural Science Foundation of China(No.29972017)
文摘A new isopropenyl benzofuran-type tetramer was isolated from the roots of ligularia stenocephala and its structure was established by spectroscopic methods.
基金This work was supported by the National Natural Science Foundation of China.
文摘From the roots of Sanguisorba alpina, a new triterpenoid was isolated and identified as 2-isobutyryloxy-19α, 25-dihydroxyursa-1, 12-dien-28-oic acid by means of spectral methods, named as aipinic acid.
基金This work was supported by the National Natural Science Foundation of China(No.29972017).
文摘Two new eremophilane sesquiterpenes, 15β-formic ether-6-oxo-furanoeremophilane (1) and 6α, 15β-epoxy eremophila-7(11)-en-8α, 12-olide (2) were isolation from the roots of Ligularia macrophylla. Their structures were deduced from spectroscopic methods and 2D NMR experiments.
基金This work was supported by the National Natural Sciencc Foundation of China No.29972017the Foundation of the Ministry of Education of China for Doctoral Program No.98073003
文摘Two new eremophilane sesquiterpenes 3β-angeloyloxy-8α-hydroxy-6β-methoxy eremophil-7 (11), 9 (10)-dien-8, 12-olide (1) and 3β-angeloyloxy-6β, 8α-dihydroxy-eremophi-7 (11), 9 (10)-dien-8, 12-olide (2) were isolated from Cacalia ainsliaeflora. Their structures were established by spectroscopic methods and 2D NMR experiments.
基金Project supported by the Nahonal Natural Sciencc Foundahon and the grant for doctoral program from State Education Commission of China
文摘Two new minor steroidal saponins, (25R) spirostan-3β-ol-6-one-3-O-[α-L- arabinopyranosyl(1-4)]-β-D-glucopyranosidc (1) and (25S) spirost-5-en -3β, 17α, 27-triol-3-O- [α-L-arabinopyranosyl(1-6)]-β-D-glucopyranosidc (2) were isolated from the roots of Smilax lebrunii. Their structures were established on thc basis of chemical and spectral methods.
文摘Chemical investigation of L.sagitta afforded two new cremophilenolides, which were identified as 6beta-angeloyloxy-10beta-hydroxy-8beta-methoxy-cremophil-7(11)-en-12, 8alpha-olide (1) and 6beta, 8beta-dimethoxy-10beta-hydroxy-eremophil-7(11)-en-12, 8alpha-olide (2). Their structures were established by spectroscopic methods including 2D NMR experiments.
基金This work was supported by the National Natural Science Foundation of China No.29972017.
文摘A new sesquiterpene and a new norsesquiterpene were isolated from the whole plant of Cacalia deltophylla (Maxim) Mattf. Their structures were elucidated as deltocacalone (1) and deltonorcacalol (2) by spectroscopic methods including 2D NMR.
基金This work was financed by The NNSFC (No. 29972017) and the FMEC (No. 98073003).
文摘A new sesquiterpene: 11,12,13-trihydroxy-4(15),7(8)-eudesmdien-9-one was isolated from Saussurea parviflora. The structure was elucidated on the basis of spectral evidence.
文摘A new xanthanolide was isolated from the aerial parts of Carpesium longifolium. Its structure was elucidated as 1, 4-epoxy-5?hydroxy-10酘-xantha-11(13)-en-12, 8?olide by spectral methods (HRMS, 1D and 2D NMR).
基金This work was supported by the National Natural Science Foundation of China No.29972017
文摘Two new eremophilenolides (3b-angeloyloxy-8b, 10b-dihydroxy-6b-ethoxyeremophile- nolide (1) and 3b, 6b-diangeloyloxy-8a-methoxy-10a-hydroxyeremophilenolide (2) were isolated from the roots of Cacalia ainsliaeflora. Their structures were elucidated by spectroscopic methods.
基金We are grateful for the financial support from the National Natural Science Foundation of China No.29972017the Foundation for Doctoral Program of Mnister of Education of China for No.98073003
文摘A new eudesmanoilde was isolated from the aerial parts of Carpesium macrocephalum. Its structure was elucidated as 2?acetoxy-11酘-eudesma-4-en-12, 8?olide by spectral methods.
文摘A New steroidal saponin was isolated from the rhizomes of Smilax lebrunii. On the basis of spectral and chemical methods, its structure was elucidated as:(25S)spirost-5-en-3β, 17α, 27-triol-3-0-[β-D-glucopyranosyl(1-4)][α-L-arabinopyranosyl(1-6)]-β-D-glucopyranoside.
基金Project supported by the National Natural Scicnce Foundation of Chinathe grant for doctoral program from State Education Commission of China
文摘Two minor steroidal saponins were isolated from the roots of Smilax menispermoidea.One of them is new and its structure was established as(25S) spirost-5-en-3β,17α,27-triol-3-O-[α-L-rhamnopyranosyl(1-4)]-β-D-gluco- pyranoside using spectroscopic and chemical methods.