Relevant bibliographies by topics / Octahydroindoles

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Octahydroindoles'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Octahydroindoles"

1

Yan, Jiahang, Wenting Zhang, Qiaoqiao He та ін. "Enantioselective direct vinylogous Michael addition for constructing enantioenriched γ,γ-dialkyl substituted butyrolactams and octahydroindoles". Organic & Biomolecular Chemistry 20, № 12 (2022): 2387–91. http://dx.doi.org/10.1039/d2ob00112h.

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A nickel(ii)/chiral N,N′-dioxide catalyzed asymmetric direct vinylogous Michael addition of unsaturated butyrolactams enables synthesizing enantioenriched γ,γ-dialkyl substituted butyrolactams and octahydroindoles.
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2

Hanessian, Stephen, Stéphane Dorich, and Juan Del Valle. "Synthesis of Functionalized Octahydroindoles Related to Daphnyphyllum Alkaloids." Synlett 25, no. 06 (2014): 799–804. http://dx.doi.org/10.1055/s-0033-1340794.

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3

Coldham, Iain, Katherine M. Crapnell, Jonathan D. Moseley, and Rémi Rabot. "Intramolecular azomethine ylide cycloaddition reactions to give octahydroindoles." Journal of the Chemical Society, Perkin Transactions 1, no. 15 (2001): 1758–63. http://dx.doi.org/10.1039/b104390k.

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4

Mena, Marisa, Josep Bonjoch, Domingo Gomez Pardo, and Janine Cossy. "Ring Expansion of Functionalized Octahydroindoles to Enantiopurecis-Decahydroquinolines†." Journal of Organic Chemistry 71, no. 16 (2006): 5930–35. http://dx.doi.org/10.1021/jo060592p.

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5

Ghirardi, Elena, Rosa Griera, Miriam Piccichè, et al. "Stereocontrolled Access to Enantiopure 7-Substituted cis- and trans-Octahydroindoles." Organic Letters 18, no. 22 (2016): 5836–39. http://dx.doi.org/10.1021/acs.orglett.6b02861.

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6

Coldham, Iain, Katherine M. Crapnell, Jonathan D. Moseley, and Remi Rabot. "ChemInform Abstract: Intramolecular Azomethine Ylide Cycloaddition Reactions to Give Octahydroindoles." ChemInform 32, no. 52 (2010): no. http://dx.doi.org/10.1002/chin.200152110.

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7

Dorich, Stephane, Juan R. Del Valle, and Stephen Hanessian. "ChemInform Abstract: Synthesis of Functionalized Octahydroindoles Related to Daphnyphyllum Alkaloids." ChemInform 45, no. 38 (2014): no. http://dx.doi.org/10.1002/chin.201438112.

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8

Reimann, Eberhard, Christian Ettmayr, and Kurt Polborn. "Angularly Substituted Octahydroindoles, Decahydroquinolines, Octahydropyrindines, and Octahydrocyclopenta[b]pyrroles by Bruylants Reaction." Monatshefte f�r Chemie / Chemical Monthly 135, no. 5 (2004): 557–79. http://dx.doi.org/10.1007/s00706-003-0136-8.

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9

Gravier-Pelletier, Christine, William Maton, Gildas Bertho, and Yves Le Merrer. "Synthesis and glycosidase inhibitory activity of enantiopure polyhydroxylated octahydroindoles and decahydroquinolines, analogs to castanospermine." Tetrahedron 59, no. 44 (2003): 8721–30. http://dx.doi.org/10.1016/j.tet.2003.09.044.

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10

Basch, Corey H., Jameson A. Brinck, Joaquin E. Ramos, Stephen A. Habay, and Glenn P. A. Yap. "Synthesis of cis-Octahydroindoles via Intramolecular 1,3-Dipolar Cycloaddition of 2-Acyl-5-aminooxazolium Salts." Journal of Organic Chemistry 77, no. 22 (2012): 10416–21. http://dx.doi.org/10.1021/jo301600p.

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Dissertations / Theses on the topic "Octahydroindoles"

1

Clarisse, Damien. "Nouvelles voies d'accès à des hétérocycles substitués : par hydrogénation d'indoles, réaction de Prins, d'aza-Prins et application à la synthèse des decytospolides A et B." Thesis, Lyon 1, 2013. http://www.theses.fr/2013LYO10179/document.

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Les hétérocycles sont des motifs présents dans un grand nombre de produits naturels et synthétiques possédant une activité biologique. Le développement de méthodes pour construire ces motifs constitue un axe de recherche important et de nombreuses voies de synthèse ont été et sont encore aujourd'hui étudiées. Au cours de ces travaux de thèse, plusieurs méthodologies ont été développées permettant l'accès à de nouveaux hétérocycles: Une première étude sur l'hydrogénation des indoles et sur l'influence de leur substitution a été réalisée. Ces travaux ont permis de mettre au point une méthode sim
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2

Guillemette, Sébastien. "Exploration du potentiel des acides 2-carboxy-6-hydroxyoctahydroindoles dans le développement d'inhibiteurs de la thrombine"." Thèse, 2006. http://hdl.handle.net/1866/16789.

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3

Shiue, Yuan-Shin, and 薛園馨. "Iron Halide-Promoted Cyclization Reaction of 6-Membered Ring 2-Enynamides and 2,3-Epoxy-1-ynamides : Stereoselective Synthesis of Octahydroindolones and Bicyclic Oxazolidines." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/6555dh.

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碩士<br>國立臺灣師範大學<br>化學系<br>104<br>Chapter I, a novel synthesis of halogenated bicyclic γ-lactams with four stereogenic centers is developed. Treatment of iron(II) halides with six-membered ring 2-enynamides in THF under dry air afforded halogenated bicyclic [4.3.0] γ-lactams in good yields. The key feature in this reaction involving an anti-addition of a halide ion and the iron center across the activated double bond. The reactions are procedurally simple, high yielding, and excellently diastereoselective, producing bicyclic γ-lactams under mild conditions without additional oxidizing agents. C
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Journal articles
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