2013
BOUGOFFA LAZHAR, MENNOUNI ABDELAZIZ, Rach RC.
Solving Cauchy integral equations of the first kind by the Adomian decomposition method. Applied Mathematics and ComputationApplied Mathematics and Computation. 2013;219 :4423-4433.
BOUGOFFA LAZHAR, MENNOUNI ABDELAZIZ, Rach RC.
Solving Cauchy integral equations of the first kind by the Adomian decomposition method. Applied Mathematics and ComputationApplied Mathematics and Computation. 2013;219 :4423-4433.
BOUGOFFA LAZHAR, MENNOUNI ABDELAZIZ, Rach RC.
Solving Cauchy integral equations of the first kind by the Adomian decomposition method. Applied Mathematics and ComputationApplied Mathematics and Computation. 2013;219 :4423-4433.
Fezzani A, Drid S, Makouf A, Alaoui CL.
Speed sensorless flatness-based control of PMSM using a second order sliding mode observer. 2013 Eighth International Conference and Exhibition on Ecological Vehicles and Renewable Energies (EVER). 2013 :1-9.
Fezzani A, Drid S, Makouf A, Alaoui CL.
Speed sensorless flatness-based control of PMSM using a second order sliding mode observer. 2013 Eighth International Conference and Exhibition on Ecological Vehicles and Renewable Energies (EVER). 2013 :1-9.
Fezzani A, Drid S, Makouf A, Alaoui CL.
Speed sensorless flatness-based control of PMSM using a second order sliding mode observer. 2013 Eighth International Conference and Exhibition on Ecological Vehicles and Renewable Energies (EVER). 2013 :1-9.
Fezzani A, Drid S, Makouf A, Alaoui CL.
Speed sensorless flatness-based control of PMSM using a second order sliding mode observer. 2013 Eighth International Conference and Exhibition on Ecological Vehicles and Renewable Energies (EVER). 2013 :1-9.
Rezgui A, Mitaine-Offer A-C, Pertuit D, Miyamoto T, Tanaka C, Delemasure S, Dutartre P, Lacaille-Dubois M-A.
Steroidal saponins from Dracaena marginata. Natural Product CommunicationsNatural Product Communications. 2013;8 :157-160.
AbstractThree new steroidal saponins and ten known ones were isolated from the bark of Dracaena marginata, along with two known steroidal saponins from the roots. Their structures were elucidated on the basis of extensive 1D and 2D NMR experiments and mass spectrometry as (25R)-26-(beta-D-glucopyranosyloxy)3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-[alpha-L-rhamnopyranosyl-(1 –> 4)]-beta-D-glucopyranoside (1), (25R)-26-(beta-D-glucopyranosyloxy)-3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (2), and (25S)-3beta-hydroxyspirost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (3).
Rezgui A, Mitaine-Offer A-C, Pertuit D, Miyamoto T, Tanaka C, Delemasure S, Dutartre P, Lacaille-Dubois M-A.
Steroidal saponins from Dracaena marginata. Natural Product CommunicationsNatural Product Communications. 2013;8 :157-160.
AbstractThree new steroidal saponins and ten known ones were isolated from the bark of Dracaena marginata, along with two known steroidal saponins from the roots. Their structures were elucidated on the basis of extensive 1D and 2D NMR experiments and mass spectrometry as (25R)-26-(beta-D-glucopyranosyloxy)3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-[alpha-L-rhamnopyranosyl-(1 –> 4)]-beta-D-glucopyranoside (1), (25R)-26-(beta-D-glucopyranosyloxy)-3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (2), and (25S)-3beta-hydroxyspirost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (3).
Rezgui A, Mitaine-Offer A-C, Pertuit D, Miyamoto T, Tanaka C, Delemasure S, Dutartre P, Lacaille-Dubois M-A.
Steroidal saponins from Dracaena marginata. Natural Product CommunicationsNatural Product Communications. 2013;8 :157-160.
AbstractThree new steroidal saponins and ten known ones were isolated from the bark of Dracaena marginata, along with two known steroidal saponins from the roots. Their structures were elucidated on the basis of extensive 1D and 2D NMR experiments and mass spectrometry as (25R)-26-(beta-D-glucopyranosyloxy)3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-[alpha-L-rhamnopyranosyl-(1 –> 4)]-beta-D-glucopyranoside (1), (25R)-26-(beta-D-glucopyranosyloxy)-3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (2), and (25S)-3beta-hydroxyspirost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (3).
Rezgui A, Mitaine-Offer A-C, Pertuit D, Miyamoto T, Tanaka C, Delemasure S, Dutartre P, Lacaille-Dubois M-A.
Steroidal saponins from Dracaena marginata. Natural Product CommunicationsNatural Product Communications. 2013;8 :157-160.
AbstractThree new steroidal saponins and ten known ones were isolated from the bark of Dracaena marginata, along with two known steroidal saponins from the roots. Their structures were elucidated on the basis of extensive 1D and 2D NMR experiments and mass spectrometry as (25R)-26-(beta-D-glucopyranosyloxy)3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-[alpha-L-rhamnopyranosyl-(1 –> 4)]-beta-D-glucopyranoside (1), (25R)-26-(beta-D-glucopyranosyloxy)-3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (2), and (25S)-3beta-hydroxyspirost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (3).
Rezgui A, Mitaine-Offer A-C, Pertuit D, Miyamoto T, Tanaka C, Delemasure S, Dutartre P, Lacaille-Dubois M-A.
Steroidal saponins from Dracaena marginata. Natural Product CommunicationsNatural Product Communications. 2013;8 :157-160.
AbstractThree new steroidal saponins and ten known ones were isolated from the bark of Dracaena marginata, along with two known steroidal saponins from the roots. Their structures were elucidated on the basis of extensive 1D and 2D NMR experiments and mass spectrometry as (25R)-26-(beta-D-glucopyranosyloxy)3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-[alpha-L-rhamnopyranosyl-(1 –> 4)]-beta-D-glucopyranoside (1), (25R)-26-(beta-D-glucopyranosyloxy)-3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (2), and (25S)-3beta-hydroxyspirost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (3).
Rezgui A, Mitaine-Offer A-C, Pertuit D, Miyamoto T, Tanaka C, Delemasure S, Dutartre P, Lacaille-Dubois M-A.
Steroidal saponins from Dracaena marginata. Natural Product CommunicationsNatural Product Communications. 2013;8 :157-160.
AbstractThree new steroidal saponins and ten known ones were isolated from the bark of Dracaena marginata, along with two known steroidal saponins from the roots. Their structures were elucidated on the basis of extensive 1D and 2D NMR experiments and mass spectrometry as (25R)-26-(beta-D-glucopyranosyloxy)3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-[alpha-L-rhamnopyranosyl-(1 –> 4)]-beta-D-glucopyranoside (1), (25R)-26-(beta-D-glucopyranosyloxy)-3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (2), and (25S)-3beta-hydroxyspirost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (3).
Rezgui A, Mitaine-Offer A-C, Pertuit D, Miyamoto T, Tanaka C, Delemasure S, Dutartre P, Lacaille-Dubois M-A.
Steroidal saponins from Dracaena marginata. Natural Product CommunicationsNatural Product Communications. 2013;8 :157-160.
AbstractThree new steroidal saponins and ten known ones were isolated from the bark of Dracaena marginata, along with two known steroidal saponins from the roots. Their structures were elucidated on the basis of extensive 1D and 2D NMR experiments and mass spectrometry as (25R)-26-(beta-D-glucopyranosyloxy)3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-[alpha-L-rhamnopyranosyl-(1 –> 4)]-beta-D-glucopyranoside (1), (25R)-26-(beta-D-glucopyranosyloxy)-3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (2), and (25S)-3beta-hydroxyspirost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (3).
Rezgui A, Mitaine-Offer A-C, Pertuit D, Miyamoto T, Tanaka C, Delemasure S, Dutartre P, Lacaille-Dubois M-A.
Steroidal saponins from Dracaena marginata. Natural Product CommunicationsNatural Product Communications. 2013;8 :157-160.
AbstractThree new steroidal saponins and ten known ones were isolated from the bark of Dracaena marginata, along with two known steroidal saponins from the roots. Their structures were elucidated on the basis of extensive 1D and 2D NMR experiments and mass spectrometry as (25R)-26-(beta-D-glucopyranosyloxy)3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-[alpha-L-rhamnopyranosyl-(1 –> 4)]-beta-D-glucopyranoside (1), (25R)-26-(beta-D-glucopyranosyloxy)-3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (2), and (25S)-3beta-hydroxyspirost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 –> 2)-4-O-sulfo-alpha-L-arabinopyranoside (3).