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Journal articles on the topic 'Lepadines'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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1

Amat, Mercedes, Alexandre Pinto, Rosa Griera, and Joan Bosch. "Stereoselective synthesis of (−)-lepadins A–C." Chemical Communications 49, no. 94 (2013): 11032. http://dx.doi.org/10.1039/c3cc46801a.

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2

Li, Xiong, Lingling Hu, Junhao Jia, He Gu, Yuanliang Jia, and Xiaochuan Chen. "A Stereoselective Approach toward (−)-Lepadins A–C." Organic Letters 19, no. 19 (2017): 5372–75. http://dx.doi.org/10.1021/acs.orglett.7b02647.

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3

Li, Gang, and Richard P. Hsung. "Assignment of the C5′ Relative Stereochemistry in (+)-Lepadin F and (+)-Lepadin G and Absolute Configuration of (+)-Lepadin G." Organic Letters 11, no. 20 (2009): 4616–19. http://dx.doi.org/10.1021/ol9018997.

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4

Amat, Mercedes, Alexandre Pinto, Rosa Griera, and Joan Bosch. "ChemInform Abstract: Stereoselective Synthesis of (-)-Lepadins A-C." ChemInform 45, no. 13 (2014): no. http://dx.doi.org/10.1002/chin.201413227.

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5

Li, Gang, Richard P. Hsung, Brian W. Slafer, and Irina K. Sagamanova. "Total Synthesis of (+)-Lepadin F." Organic Letters 10, no. 21 (2008): 4991–94. http://dx.doi.org/10.1021/ol802068q.

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6

Davis, Rohan A., Anthony R. Carroll, and Ronald J. Quinn. "Lepadins F−H, Newcis-Decahydroquinoline Alkaloids from the Australian AscidianAplidiumtabascum." Journal of Natural Products 65, no. 4 (2002): 454–57. http://dx.doi.org/10.1021/np010407x.

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7

Amat, Mercedes, Alexandre Pinto, Rosa Griera, and Joan Bosch. "Enantioselective Synthesis of Lepadins A-D from a Phenylglycinol-Derived Hydroquinolone Lactam." Chemistry - A European Journal 21, no. 36 (2015): 12804–8. http://dx.doi.org/10.1002/chem.201501909.

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8

Wright, Anthony D., Eva Goclik, Gabriele M. König, and Ronald Kaminsky. "Lepadins D−F: Antiplasmodial and Antitrypanosomal Decahydroquinoline Derivatives from the Tropical Marine TunicateDidemnumsp." Journal of Medicinal Chemistry 45, no. 14 (2002): 3067–72. http://dx.doi.org/10.1021/jm0110892.

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9

Ozawa, Tetsuji, Sakae Aoyagi, and Chihiro Kibayashi. "Total Synthesis of the Marine Alkaloid (−)-Lepadin B." Organic Letters 2, no. 19 (2000): 2955–58. http://dx.doi.org/10.1021/ol000153r.

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10

Pu, Xiaotao, and Dawei Ma. "Facile Entry to Substituted Decahydroquinoline Alkaloids. Total Synthesis of Lepadins A−E and H." Journal of Organic Chemistry 71, no. 17 (2006): 6562–72. http://dx.doi.org/10.1021/jo061070c.

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11

Toyooka, Naoki, Maiko Okumura, and Hiroki Takahata. "Enantioselective Total Synthesis of the Marine Alkaloid Lepadin B." Journal of Organic Chemistry 64, no. 7 (1999): 2182–83. http://dx.doi.org/10.1021/jo990141n.

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12

Ma, Foqing, Chenxi He, Eryu Wang, and Rongbiao Tong. "Collective Asymmetric Total Syntheses of Marine Decahydroquinoline Alkaloid Lepadins A–E, H, and ent-I." Organic Letters 23, no. 16 (2021): 6583–88. http://dx.doi.org/10.1021/acs.orglett.1c02435.

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13

KANTVILAS, GINTARAS. "Tasmanian chroodiscoid thelotremoid lichens (Graphidaceae) revisited." Phytotaxa 459, no. 3 (2020): 209–18. http://dx.doi.org/10.11646/phytotaxa.459.3.2.

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Some thelotremoid lichens of Tasmania are reviewed. The following new combinations are proposed: Gintarasia asteliae (Kantvilas & Vĕzda) Kantvilas, G. minor (Kantvilas & Vĕzda) Kantvilas and G. tasmanica (Kantvilas & Vĕzda) Kantvilas. A revised description of Schizotrema schizolomum (Müll.Arg.) Mangold & Lumbsch, based on Tasmanian collections, is provided, and the new species, S. vezdanum Kantvilas, recorded from Tasmanian and Victoria, is described and illustrated; it is characterised by a thallus containing stictic acid, 8-spored asci, and non-amyloid, muriform ascospores, 2

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14

Steffan, Bert. "Lepadin A, A decahydroquinoline alkaloid from the tunicate Clavelina lepadiformis." Tetrahedron 47, no. 41 (1991): 8729–32. http://dx.doi.org/10.1016/s0040-4020(01)96194-0.

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15

Ozawa, Tetsuji, Sakae Aoyagi, and Chihiro Kibayashi. "ChemInform Abstract: Total Synthesis of the Marine Alkaloid (-)-Lepadin B." ChemInform 32, no. 1 (2001): no. http://dx.doi.org/10.1002/chin.200101217.

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16

Wright, Anthony D., Eva Goclik, Gabriele M. Koenig, and Ronald Kaminsky. "ChemInform Abstract: Lepadins D-F: Antiplasmodial and Antitrypanosomal Decahydroquinoline Derivatives from the Tropical Marine Tunicate Didemnum sp." ChemInform 33, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.200250178.

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17

Tsuneki, Hiroshi, Yueren You, Naoki Toyooka, et al. "Marine Alkaloids (−)-Pictamine and (−)-Lepadin B Block Neuronal Nicotinic Acetylcholine Receptors." Biological & Pharmaceutical Bulletin 28, no. 4 (2005): 611–14. http://dx.doi.org/10.1248/bpb.28.611.

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18

Toyooka, Naoki, Maiko Okumura, and Hiroki Takahata. "ChemInform Abstract: Enantioselective Total Synthesis of the Marine Alkaloid Lepadin B." ChemInform 30, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.199931246.

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19

Pu, Xiaotao, and Dawei Ma. "Total Synthesis of Lepadins B, D, E, and H; Determination of the Configuration of the Latter Three Alkaloids." Angewandte Chemie International Edition 43, no. 32 (2004): 4222–25. http://dx.doi.org/10.1002/anie.200460128.

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20

Pu, Xiaotao, and Dawei Ma. "Total Synthesis of Lepadins B, D, E, and H; Determination of the Configuration of the Latter Three Alkaloids." Angewandte Chemie 116, no. 32 (2004): 4318–21. http://dx.doi.org/10.1002/ange.200460128.

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21

STEFFAN, B. "ChemInform Abstract: Lepadin A, a Decahydroquinoline Alkaloid from the Tunicate Clavelina lepadiformis." ChemInform 23, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199206279.

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22

Ozawa, Tetsuji, Sakae Aoyagi, and Chihiro Kibayashi. "Total Synthesis of the Marine Alkaloids (−)-Lepadins A, B, and C Based on Stereocontrolled Intramolecular Acylnitroso-Diels−Alder Reaction." Journal of Organic Chemistry 66, no. 10 (2001): 3338–47. http://dx.doi.org/10.1021/jo001589n.

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23

Pelss, A., and A. M. P. Koskinen. "ChemInform Abstract: Stereocontrolled Construction of Decahydroquinoline Ring Systems: The Case of Lepadin Alkaloids." ChemInform 44, no. 38 (2013): no. http://dx.doi.org/10.1002/chin.201338224.

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24

Pelss, A., and A. M. P. Koskinen. "Stereocontrolled construction of decahydro quinoline ring systems: the case of lepadin alkaloids (Review)." Chemistry of Heterocyclic Compounds 49, no. 2 (2013): 226–40. http://dx.doi.org/10.1007/s10593-013-1239-8.

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25

Ómarsdóttir, Sesselja, Xiao Wang, Hong-bing Liu, Brendan M. Duggan, and Tadeusz F. Molinski. "Lepadins I–K, 3-O-(3′-Methylthio)acryloyloxy-decahydroquinoline Esters from a Bahamian Ascidian Didemnum sp. Assignment of Absolute Stereostructures." Journal of Organic Chemistry 83, no. 22 (2018): 13670–77. http://dx.doi.org/10.1021/acs.joc.8b01609.

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26

Barbe, Guillaume, and André B. Charette. "Total Synthesis of (+)-Lepadin B: Stereoselective Synthesis of Nonracemic Polysubstituted Hydroquinolines Using an RC-ROM Process." Journal of the American Chemical Society 130, no. 42 (2008): 13873–75. http://dx.doi.org/10.1021/ja8068215.

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27

Ozawa, Tetsuji, Sakae Aoyagi, and Chihiro Kibayashi. "ChemInform Abstract: Total Synthesis of the Marine Alkaloids (-)-Lepadins A (X), B (IX), and C (XI) Based on Stereocontrolled Intramolecular Acylnitroso-Diels-Alder Reaction." ChemInform 32, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.200138193.

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28

Mena, Marisa, and Josep Bonjoch. "Model studies in the lepadin series: synthesis of enantiopure decahydroquinolines by aminocyclization of 2-(3-aminoalkyl)cyclohexenones." Tetrahedron 61, no. 34 (2005): 8264–70. http://dx.doi.org/10.1016/j.tet.2005.06.024.

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29

Niethe, Alexander, Dirk Fischer, and Siegfried Blechert. "Total Synthesis of ent-Lepadin F and G by a Tandem Ene−Yne−Ene Ring Closing Metathesis." Journal of Organic Chemistry 73, no. 8 (2008): 3088–93. http://dx.doi.org/10.1021/jo7027079.

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30

Kalai, Chakib, Edward Tate, and Samir Z. Zard. "ChemInform Abstract: A Short Formal Route to (.+-.)-Lepadin B Using a Xanthate-Mediated Free Radical Cyclization/Vinylaton Sequence." ChemInform 33, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.200244217.

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31

Hsung, Richard, Gang Li, Lauren Carlson, et al. "Stereodivergent Approach to Both C2,8a-syn and C2,8a-anti Relative Stereochemical Manifolds in the Lepadin Family via a TiCl4-Promoted Aza-[3+3] Annulation." Synthesis 2009, no. 17 (2009): 2905–14. http://dx.doi.org/10.1055/s-0029-1216920.

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32

Toyooka, Naoki, Maiko Okumura, Hiroki Takahata, and Hideo Nemoto. "Construction of 4a,8a-cis-octahydroquinolin-7-one core using an intramolecular aldol type of cyclization: An application to enantioselective total synthesis of lepadin B." Tetrahedron 55, no. 35 (1999): 10673–84. http://dx.doi.org/10.1016/s0040-4020(99)00603-1.

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33

Toyooka, Naoki, Maiko Okumura, Hiroki Takahata, and Hideo Nemoto. "ChemInform Abstract: Construction of 4a,8a-cis-Octahydroquinolin-7-one Core Using an Intramolecular Aldol Type of Cyclization: An Application to the Enantioselective Total Synthesis of Lepadin B." ChemInform 30, no. 47 (2010): no. http://dx.doi.org/10.1002/chin.199947226.

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34

Kalaï, Chakib, Edward Tate, and Samir Z. Zard. "A short formal route to (±)-lepadin B using a xanthate-mediated free radical cyclisation/vinylation sequenceElectronic supplementary information (ESI) available: experimental and characterisation data for the transformation of 13 and 14. See http://www.rsc.org/suppdata/cc/b2/b203604e/." Chemical Communications, no. 13 (June 5, 2002): 1430–31. http://dx.doi.org/10.1039/b203604e.

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35

"Synthesis of (+)-Lepadin F." Synfacts 2009, no. 06 (2009): 0590. http://dx.doi.org/10.1055/s-0029-1216675.

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36

"Synthesis of (+)-Lepadin B." Synfacts 2009, no. 04 (2009): 0359. http://dx.doi.org/10.1055/s-0028-1088089.

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37

"Synthesis of ent-Lepadin F." Synfacts 2008, no. 10 (2008): 1020. http://dx.doi.org/10.1055/s-2008-1078182.

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38

Li, Gang, Richard P. Hsung, Brian W. Slafer, and Irina K. Sagamanova. "ChemInform Abstract: Total Synthesis of (+)-Lepadin F." ChemInform 40, no. 12 (2009). http://dx.doi.org/10.1002/chin.200912198.

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39

Pu, Xiaotao, and Dawei Ma. "Facile Entry to Substituted Decahydroquinoline Alkaloids. Total Synthesis of Lepadins A—E and H." ChemInform 38, no. 2 (2007). http://dx.doi.org/10.1002/chin.200702189.

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40

Matwiejuk, Anna. "New records of Skyttea nitschkei from the Augustów Forest in Poland." Acta Mycologica 51, no. 1 (2016). http://dx.doi.org/10.5586/am.1078.

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The paper presents data about an interesting lichenicolous fungus <em>Skyttea nitschkei</em> (Körb.) Sherwood, D. Hawksw. &amp; Coppins reported for the first time from Poland. Material described was collected by the author in 2014 in the Augustów Forest on thalli of <em>Thelotrema lepadinum</em> grown on the bark of <em>Quercus robur</em>. The stand was located in moist fertile oak-linden-hornbeam forest <em>Tilio-Carpinetum</em> with old <em>Q. robur</em>, <em>Carpinus betulus</em>, <em>Alnus glutinosa</em&g

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41

Pu, Xiaotao, and Dawei Ma. "Total Synthesis of Lepadins B, D, E, and H; Determination of the Configuration of the Latter Three Alkaloids (II)." ChemInform 35, no. 49 (2004). http://dx.doi.org/10.1002/chin.200449191.

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42

Gu, He, Yue Hu, Yuanliang Jia, Qin Zhou, Guiyin Luo, and Xiaochuan Chen. "Total Synthesis of (‐)‐Lepadin F based on a stereoselective Diels‐Alder reaction controlled by a ketolactone‐type dienophile." Chemistry – A European Journal, December 2, 2020. http://dx.doi.org/10.1002/chem.202004778.

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43

Barbe, Guillaume, and Andre B. Charette. "ChemInform Abstract: Total Synthesis of (+)-Lepadin B (III): Stereoselective Synthesis of Nonracemic Polysubstituted Hydroquinolines Using an RC-ROM Process." ChemInform 40, no. 9 (2009). http://dx.doi.org/10.1002/chin.200909205.

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44

Niethe, Alexander, Dirk Fischer, and Siegfried Blechert. "ChemInform Abstract: Total Synthesis of ent-Lepadin F (IIIa) and G (IIIb) by a Tandem Ene-Yne-Ene Ring Closing Metathesis." ChemInform 39, no. 35 (2008). http://dx.doi.org/10.1002/chin.200835186.

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