(Q104948086)

http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900492-0

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1-methyl-3H,4H,9H-pyrido[3,4-b]indole

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methyl (1S,10S,12S,13E,18R)-13-ethylidene-18-(hydroxymethyl)-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate

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12-Methoxypleiocarpine

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(12S,19R)-12-ethyl-19-hydroxy-8,16-diazatetracyclo[10.6.1.02,7.016,19]nonadeca-1(18),2,4,6-tetraene-9,17-dione

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methyl (1R,9R,16R,18R,21S)-2,12-diazahexacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸.0¹⁶,²¹]henicosa-3,5,7-triene-18-carboxylate

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(8R,15S,19R)-15-ethyl-1,11-diazapentacyclo[9.7.1.02,7.08,19.015,19]nonadeca-2,4,6-triene-10,18-dione

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dimethyl (1R,9S,16R,19R,20S)-4-methoxy-21-oxo-2,12-diazahexacyclo[10.6.2.19,16.01,9.03,8.016,20]henicosa-3(8),4,6-triene-2,19-dicarboxylate

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(12R,19S)-12-ethyl-9,19-dihydroxy-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(18),2,4,6,8-pentaen-17-one

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2,18-dimethyl (1R,9R,16R,18R,21S)-2,12-diazahexacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸.0¹⁶,²¹]henicosa-3,5,7-triene-2,18-dicarboxylate

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methyl (1S,10S,12S,13E,15R,18R)-13-ethylidene-18-(hydroxymethyl)-15-oxido-8-aza-15-azoniapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate

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dimethyl (1S,9R,16R,18S,21S)-18-hydroxy-4-methoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-2,18-dicarboxylate

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methyl 2-[(3E)-3-ethylidene-1H,2H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-2-yl]-2-{1H,2H,3H,4H,9H-pyrido[3,4-b]indol-1-yl}acetate

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methyl (1S,10S,12S,13E,15R,18R)-18-(acetyloxymethyl)-13-ethylidene-15-oxido-8-aza-15-azoniapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate

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Methyl 13-ethylidene-18-(hydroxymethyl)-8,15-diazapentacyclo[10.5.1.01,9.02,7.010,15]octadeca-2,4,6,8-tetraene-18-carboxylate

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1 reference

Dimethyl 4-methoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-2,18-dicarboxylate

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3'-Ethyl-1',3-ethano-1,3'-propanospiro[1H-indole-2(3H),2'-piperidine]-9',10'-dione

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Dimethyl 4-methoxy-21-oxo-2,12-diazahexacyclo[10.6.2.19,16.01,9.03,8.016,20]henicosa-3(8),4,6-triene-2,19-dicarboxylate

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1 reference

Dimethyl 18-hydroxy-4-methoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-2,18-dicarboxylate

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1 reference

Dimethyl 21-hydroxy-5,7-dioxa-2,15-diazaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9-triene-2,21-dicarboxylate

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Dimethyl 2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-2,18-dicarboxylate

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Phelipanche aegyptiaca

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Toh-Seok Kam

1

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900492-0

Kooi-Mow Sim

series ordinal

2

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900492-0

Takashi Koyano

series ordinal

3

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900492-0

Kanki Komiyama

series ordinal

4

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900492-0

publication date

January 1999

3 references

16 September 2022

16 September 2022

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900492-0

volume

50

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900492-0

page(s)

75-79

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issue

1

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900492-0

cites work

Indole alkaloids from leaves and stems of Leuconotis eugenifolius

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7 January 2021

Lapidilectine A and lapidilectine B, two new alkaloids from Kopsia lapidilecta

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900492-0

7 January 2021

Alkaloids from stem bark and leaves of Peschiera buchtieni

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900492-0

7 January 2021

[Monomeric Indole Alkaloids from Kopsia officinalis.].

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7 January 2021

Plumeran alkaloids from Kopsia profunda

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7 January 2021

Alkaloids from leaves of Kopsia larutensis

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900492-0

7 January 2021

Absolute configuration of C-16 of eburnane alkaloids from Kopsia larutensis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900492-0

7 January 2021

Lundurines A, B and C, new indole alkaloids with a novel carbon skeleton containing a cyclopropyl moiety

1 reference

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7 January 2021

Paucidactine A and B, new indole alkaloids with a novel ring system containing a lactone moiety

1 reference

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7 January 2021

Novel Cage Indoles from a MalaysianKopsia

1 reference

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7 January 2021

Tenuisines A, B and C, novel bisindoles with C2 symmetry from Kopsia tenuis

1 reference

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7 January 2021

Pauciflorines A and B, novel melanin biosynthesis inhibitors from Kopsia

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7 January 2021

Alkaloids from Kopsia griffithii

1 reference

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7 January 2021

A new antileishmanial compound, phaseolinone

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7 January 2021

A preliminary chemotaxonomic review of Kopsia (Apocynaceae).

1 reference

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7 January 2021

Terengganensines A and B, dihydroeburnane alkaloids from Kopsia terengganensis

1 reference

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7 January 2021

Indolalkaloide aus Conopharyngia durissima STAPF. 134. Mitteilung über Alkaloide [1]

1 reference

COCI

https://opencitations.net/index/api/v1/citations/10.1002/HLCA.19690520318