2014
DOI: 10.1016/j.tet.2014.08.042
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Three new Lycopodium alkaloids from Huperzia carinata and Huperzia squarrosa

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Cited by 31 publications
(45 citation statements)
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“…Lycopodium alkaloids (Fig. 2) have been isolated and reported from 13 Huperziaceae species and varieties (Table 1) (Tong et al 2003b) 12-Epilycodoline N-oxide H. serrata ) 4,6-Dihydroxyserratidine H. serrata (Tan et al 2002d) 4-Hydroxyserratidine H. serrata (Tan et al 2002d) 4,6-Dihydroxylycopodine H. serrata 6-Hydroxylycopodine H. serrata (Yuan et al 1995) 6-Hydroxyserratidine H. serrata (Tan et al 2002d) 7-Hydroxylycopodine H. serrata Phytochem Rev (2017) 16:379-440 381 (Tong et al 2003b) Flabelliformine H. miyoshiana (Tong et al 2003b) Gnidioidine H. carinata (Thorroad et al 2014) Huperzine E H. serrata (Zhu et al 1996;Wang et al 2001) Huperzine F H. serrata (Zhu et al 1996;Wang et al 2001) Huperzine G H. serrata (Wang et al 1998(Wang et al , 2000 Huperzine O H. serrata (Wang et al 2000) Lucidioline H. serrata (Zhou et al 1993;Ma et al 1998) Lycocarinatine A H. carinata (Thorroad et al 2014) Lycodoline H. miyoshiana (Tong et al 2003b), H. serrata (Yuan et al 1995), H. carinata (Thorroad et al 2014) Lycopodine H. miyoshiana (Tong et al 2003b), H. serrata (Yuan et al 1995) Lycoposerramine K H. carinata (Thorroad et al 2014) Lycoposerramine U N-oxide H. squarrosa (Thorroad et al 2014) Miyoshianine A H. miyoshiana (Tong et al 2003b) Miyoshianine B…”
Section: Lycopodium Alkaloidsmentioning
confidence: 99%
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“…Lycopodium alkaloids (Fig. 2) have been isolated and reported from 13 Huperziaceae species and varieties (Table 1) (Tong et al 2003b) 12-Epilycodoline N-oxide H. serrata ) 4,6-Dihydroxyserratidine H. serrata (Tan et al 2002d) 4-Hydroxyserratidine H. serrata (Tan et al 2002d) 4,6-Dihydroxylycopodine H. serrata 6-Hydroxylycopodine H. serrata (Yuan et al 1995) 6-Hydroxyserratidine H. serrata (Tan et al 2002d) 7-Hydroxylycopodine H. serrata Phytochem Rev (2017) 16:379-440 381 (Tong et al 2003b) Flabelliformine H. miyoshiana (Tong et al 2003b) Gnidioidine H. carinata (Thorroad et al 2014) Huperzine E H. serrata (Zhu et al 1996;Wang et al 2001) Huperzine F H. serrata (Zhu et al 1996;Wang et al 2001) Huperzine G H. serrata (Wang et al 1998(Wang et al , 2000 Huperzine O H. serrata (Wang et al 2000) Lucidioline H. serrata (Zhou et al 1993;Ma et al 1998) Lycocarinatine A H. carinata (Thorroad et al 2014) Lycodoline H. miyoshiana (Tong et al 2003b), H. serrata (Yuan et al 1995), H. carinata (Thorroad et al 2014) Lycopodine H. miyoshiana (Tong et al 2003b), H. serrata (Yuan et al 1995) Lycoposerramine K H. carinata (Thorroad et al 2014) Lycoposerramine U N-oxide H. squarrosa (Thorroad et al 2014) Miyoshianine A H. miyoshiana (Tong et al 2003b) Miyoshianine B…”
Section: Lycopodium Alkaloidsmentioning
confidence: 99%
“…H. miyoshiana (Tong et al 2003b) Phlegmariurine B H. carinata (Thorroad et al 2014), H. squarrosa (Thorroad et al 2014) Sauroine H. saururus (Ortega et al 2004) Selagoline H. selago (Staerk et al 2004) Serratidine H. serrata (Tan et al 2002d), H. selago (Staerk et al 2004) II. Lycodine class 12-Epilycodine N-oxide H. squarrosa (Thorroad et al 2014) 6-Hydroxyhuperzine A H. serrata (Yuan and Zhao 2000) 8,15-Dihydrohuperzine A H. carinata (Thorroad et al 2014) Des-N-methyl-obscurine H. serrata (Yuan et al 1995) Huperserine E H. serrata Huperzine A H. serrata (Liu et al 1986a, b), H. selago (Staerk et al 2004), H. carinata (Thorroad et al 2014), Huperzia squarrosa (Thorroad et al 2014) Huperzine B…”
Section: Lycopodium Alkaloidsmentioning
confidence: 99%
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“…Other isolated compounds from the crude alkaloidal fraction were lycopodine, 31) lycocarinatine A, 28) 12-epi-lycodoline N-oxide, 32) lycofoline, 30) anhydrolycodoline, 30) obscurumine C, 33) gnidioidine, 30) malycorin B, 29) fawcettimine, 34) lycoposerramine-C, 35) lycoposerramine-D, 35) lycoposerramine-P, 35) phlegmariurine A, 22) phlegmariurine B, 36) huperzine A, 5) huperzine C, 37) 13N-formyl huperzine A, 38) lycodoline, 32,39) and Chemical Conversion of Lycopocarinamine A (1) into Lycopocarinamine B (2) To a solution of lycopocarinamine A (1, 1.0 mg) in MeOH (0.5 mL) was added freshly prepared ether solution of CH 2 N 2 (excess). The mixture was stirred for 1 h at room temperature.…”
Section: Experimental Generalmentioning
confidence: 99%
“…In this paper, we describe the structure elucidation of six new Lycopodium alkaloids having the lycopodine-type skeleton, which were isolated from L. carinatum, 27) and the structure revision of reported alkaloid lycocarinatine A. 28) …”
mentioning
confidence: 99%