Academic literature on the topic 'Meyers' bicyclic lactams'

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Journal articles on the topic "Meyers' bicyclic lactams"

1

Kalaitzakis, Dimitris, Tamsyn Montagnon, Ioanna Alexopoulou, and Georgios Vassilikogiannakis. "A Versatile Synthesis of Meyers' Bicyclic Lactams from Furans: Singlet-Oxygen-Initiated Reaction Cascade." Angewandte Chemie (International ed. in English) 51, no. 35 (2012): 8868–71. https://doi.org/10.1002/anie.201204419.

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All in one: Meyers' bicyclic lactams were synthesized in high yield from furans using a new and powerful method that involves a one-pot singlet-oxygen-initiated reaction cascade. This method has broad synthetic potential because of the ease of access to a wide range of furans with a variety of substituents.
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2

Penhoat, Maël, Vincent Levacher, and Georges Dupas. "Novel Extension of Meyers' Methodology: Stereoselective Construction of Axially Chiral 7,5-Fused Bicyclic Lactams†." Journal of Organic Chemistry 68, no. 24 (2003): 9517–20. http://dx.doi.org/10.1021/jo035195i.

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3

Kalaitzakis, Dimitris, Tamsyn Montagnon, Ioanna Alexopoulou, and Georgios Vassilikogiannakis. "A Versatile Synthesis of Meyers’ Bicyclic Lactams from Furans: Singlet-Oxygen-Initiated Reaction Cascade." Angewandte Chemie 124, no. 35 (2012): 8998–9001. http://dx.doi.org/10.1002/ange.201204419.

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4

Kalaitzakis, Dimitris, Tamsyn Montagnon, Ioanna Alexopoulou, and Georgios Vassilikogiannakis. "A Versatile Synthesis of Meyers’ Bicyclic Lactams from Furans: Singlet-Oxygen-Initiated Reaction Cascade." Angewandte Chemie International Edition 51, no. 35 (2012): 8868–71. http://dx.doi.org/10.1002/anie.201204419.

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5

Claudio-Catalán, Miguel Ángel, Miguel-Ángel Reyes-González, and Mario Ordóñez. "A versatile synthesis of bicyclic lactams from 1,8-naphthalaldehydic acid: an extension of Meyers’ method." Arkivoc 2013, no. 4 (2013): 413–23. http://dx.doi.org/10.3998/ark.5550190.p008.321.

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6

Kalaitzakis, Dimitris, Tamsyn Montagnon, Ioanna Alexopoulou, and Georgios Vassilikogiannakis. "ChemInform Abstract: A Versatile Synthesis of Meyers′ Bicyclic Lactams from Furans: Singlet-Oxygen-Initiated Reaction Cascade." ChemInform 44, no. 4 (2013): no. http://dx.doi.org/10.1002/chin.201304080.

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7

Penhoat, Maël, Stephane Leleu, Georges Dupas, Cyril Papamicaël, Francis Marsais, and Vincent Levacher. "Meyers’ bicyclic lactam formation under mild and highly stereoselective conditions." Tetrahedron Letters 46, no. 48 (2005): 8385–89. http://dx.doi.org/10.1016/j.tetlet.2005.09.154.

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8

Shen, Xin, Yi-Kang Wu, and Fan Zhang. "A Formal Synthesis of (+)-Cassiol Exploiting Meyers' Bicyclic Lactam Methodology." Chinese Journal of Chemistry 20, no. 11 (2010): 1439–44. http://dx.doi.org/10.1002/cjoc.20020201148.

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9

Grinev, Vyacheslav S., Elena I. Linkova, Mikhail N. Krainov, Maksim V. Dmitriev, and Alevtina Yu Yegorova. "Crystal structures, packing features, Hirshfeld surface analyses and DFT calculations of hydrogen-bond energy of two homologous 8a-aryl-2,3,4,7,8,8a-hexahydropyrrolo[1,2-a]pyrimidin-6(1H)-ones." Acta Crystallographica Section C Structural Chemistry 76, no. 5 (2020): 483–89. http://dx.doi.org/10.1107/s2053229620005409.

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The crystal structures and packing features of two homologous Meyer's bicyclic lactams with fused pyrrolidone and medium-sized perhydropyrimidine rings, namely, 8a-phenyl-2,3,4,7,8,8a-hexahydropyrrolo[1,2-a]pyrimidin-6(1H)-one, C13H16N2O (1), and 8a-(4-methylphenyl)-2,3,4,7,8,8a-hexahydropyrrolo[1,2-a]pyrimidin-6(1H)-one, C14H18N2O (2), were elucidated, and Hirshfeld surface plots were calculated and drawn for visualization and a deeper analysis of the intermolecular noncovalent interactions. Molecules of 1 and 2 are weakly linked by intermolecular C=O...H—N hydrogen bonds into chains, which a
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10

Penhoat, Maël, Pierre Bohn, Georges Dupas, Cyril Papamicaël, Francis Marsais, and Vincent Levacher. "New development of Meyers’ methodology: stereoselective preparation of an axially chiral 5,7-fused bicyclic lactam related to circumdatins/benzomalvins and asperlicins." Tetrahedron: Asymmetry 17, no. 2 (2006): 281–86. http://dx.doi.org/10.1016/j.tetasy.2005.12.019.

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