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Journal articles on the topic 'Erysotramidine'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Simpkins, Nigel S., Alexander J. Blake, Christopher Gill, Daniel A. Greenhalgh, and Fengzhi Zhang. "An Asymmetric Synthesis of (+)-Erysotramidine." Synthesis, no. 19 (2005): 3287–92. http://dx.doi.org/10.1055/s-2005-918478.

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2

L’Homme, Chloé, Marc-André Ménard, and Sylvain Canesi. "Synthesis of the Erythrina Alkaloid Erysotramidine." Journal of Organic Chemistry 79, no. 17 (2014): 8481–85. http://dx.doi.org/10.1021/jo501583c.

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3

Ju, Xiaolin, Xiaojun Hu, Hongliang Shi, et al. "Brønsted acid and Lewis acid co-promoted cascade cyclization reaction and application to the total synthesis of Erysotramidine." Organic Chemistry Frontiers 8, no. 17 (2021): 4839–44. http://dx.doi.org/10.1039/d1qo00668a.

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A strategy for the syntheses of pyrrolo [2,1-a] isoquinolines and indolizinoindolones via a Brønsted acid and Lewis acid co-promoted cascade reaction has been developed. The strategy was exemplified in the total synthesis of Erysotramidine.

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4

L'Homme, Chloe, Marc-Andre Menard, and Sylvain Canesi. "ChemInform Abstract: Synthesis of the Erythrina Alkaloid Erysotramidine." ChemInform 46, no. 11 (2015): no. http://dx.doi.org/10.1002/chin.201511276.

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5

Tietze, Lutz F., Nina Tölle, Daniel Kratzert, and Dietmar Stalke. "Efficient Formal Total Synthesis of the Erythrina Alkaloid (+)-Erysotramidine, Using a Domino Process." Organic Letters 11, no. 22 (2009): 5230–33. http://dx.doi.org/10.1021/ol901980u.

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6

Paladino, Marco, Joshua Zaifman, and Marco A. Ciufolini. "Total Synthesis of (+)-3-Demethoxyerythratidinone and (+)-Erysotramidine via the Oxidative Amidation of a Phenol." Organic Letters 17, no. 14 (2015): 3422–25. http://dx.doi.org/10.1021/acs.orglett.5b01423.

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7

Lee, Hyoung Ik, Michael P. Cassidy, Paitoon Rashatasakhon, and Albert Padwa. "Efficient Synthesis of (±)-Erysotramidine Using an NBS-Promoted Cyclization Reaction of a Hexahydroindolinone Derivative." Organic Letters 5, no. 26 (2003): 5067–70. http://dx.doi.org/10.1021/ol036106r.

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8

Padwa, Albert, Hyoung Ik Lee, Paitoon Rashatasakhon, and Mickea Rose. "Electrophilic-Induced Cyclization Reaction of Hexahydroindolinone Derivatives and Its Application toward the Synthesis of (±)-Erysotramidine." Journal of Organic Chemistry 69, no. 24 (2004): 8209–18. http://dx.doi.org/10.1021/jo048647f.

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9

Gao, Shuanhu, Yong Qiang Tu, Xiangdong Hu, et al. "General and Efficient Strategy for Erythrinan and Homoerythrinan Alkaloids: Syntheses of (±)-3-Demethoxyerythratidinone and (±)-Erysotramidine." Organic Letters 8, no. 11 (2006): 2373–76. http://dx.doi.org/10.1021/ol0607185.

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10

Mostowicz, Danuta, Mirosław Dygas, and Zbigniew Kałuża. "Heck Cyclization Strategy for Preparation of Erythrinan Alkaloids: Asymmetric Synthesis of Unnatural (−)-Erysotramidine fromL-Tartaric Acid." Journal of Organic Chemistry 80, no. 3 (2015): 1957–63. http://dx.doi.org/10.1021/jo5026157.

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11

SANO, TAKEHIRO, JUN TODA, NORIAKI KASHIWABA, TAKESHI OHSHIMA, and YOSHISUKE TSUDA. "Synthesis of Erythrina and related alkaloids. XVI Diels-Alder approach : Total synthesis of dl-erysotrine, dl-erythraline, dl-erysotramidine, dl-8-oxoerythraline and their 3-epimers." CHEMICAL & PHARMACEUTICAL BULLETIN 35, no. 2 (1987): 479–500. http://dx.doi.org/10.1248/cpb.35.479.

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12

Canesi, Sylvain. "Rapid Formation of Advanced Scaffolds from Phenols and Anilines." Synlett 30, no. 06 (2018): 647–64. http://dx.doi.org/10.1055/s-0037-1610340.

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This article is an account of our efforts over the last decade to functionalize phenols and anilines at any position and to use these compounds to generate substituted aromatic systems and advanced unsaturated cyclohexanone moieties, enabling the rapid formation of complex structures. Total syntheses of numerous natural products involving such intermediates were achieved.1 Introduction2 ortho-Functionalization of Phenols and Aniline Derivatives Mediated by Iodanes (III) and Synthesis of Panacene2.1 Cross-Coupling with Aniline Derivatives2.2 Dearomative Cycloaddition of Arenes and Heteroarenes2

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13

SHIV, K. SHARMA, та MOHINDRA CHAWLA H. "Structure Elucidation of Erythrosotidienone and Erythromotidienone- Two New Isoquinoline Alkaloids from Erythrinα vαriegαtα Flowers". Journal of Indian Chemical Society Vol. 75, Oct-Dec 1998 (1998): 833–37. https://doi.org/10.5281/zenodo.5924029.

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Department of Chemistry, Indian Institute of Technology, Hauz khas, New Delhi-110<strong> </strong>016<em> </em> <em>Manuscript received 9 November 1998</em> Careful examination of the acetone extract of the <em>Erythrinα vαriegαtα</em><em> </em>flowers has revealed the presence of five compounds, three of which are identified as stigmasterol (1), cycloartenol (2) and erysotramidinc (13). The remaining two compounds are new isoquinolines whose structures have been established on the basis of chemical correlation, derivatization and ir, <sup>1</sup>H nmr, <sup>

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14

"Formal Synthesis of (+)-Erysotramidine." Synfacts 2010, no. 04 (2010): 0392. http://dx.doi.org/10.1055/s-0029-1219452.

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15

Blake, Alexander J., Christopher Gill, Daniel A. Greenhalgh, Nigel S. Simpkins, and Fengzhi Zhang. "An Asymmetric Synthesis of (+)-Erysotramidine." ChemInform 37, no. 18 (2006). http://dx.doi.org/10.1002/chin.200618202.

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16

Zeng, Wei-Long, Xu Jiang, and Wei Li. "Chromium-Promoted Dearomative (Deutero)Hydrocyanoalkylation of (Hetero)Arenes Using Simple Alkylnitriles." Synlett, October 2, 2023. http://dx.doi.org/10.1055/a-2185-0581.

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Herein, a general strategy for regioselective dearomative 1,2-hydrocyanoalkylation of chromium-bound (hetero)arenes with simple alkylnitriles as pronucleophiles was disclosed, providing rapid access to 1,3-cyclohexadienes possessing useful alkylnitrile groups. The versatility of this methodology further enabled a selective dearomative deuteration reaction. Finally, synthetic applications of the method in the formal synthesis of natural products, including erysotramidine, demethoxyerythratidinone, and morphine, were demonstrated.

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17

Kalaitzakis, Dimitris, Tamsyn Montagnon, Eirini Antonatou, and Georgios Vassilikogiannakis. "One-pot Synthesis of the Tetracyclic Framework of the Aromatic Erythrina Alkaloids from Simple Furans." July 8, 2013. https://doi.org/10.1021/ol401582e.

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Conversion of a simple furan into the intact erythrinane skeleton in one synthetic operation has been accomplished. The one-pot reaction sequence begins with singlet oxygen photooxygenation of the furan and proceeds via a 2-pyrrolidinone formation, cyclization of the pendant aldehyde moiety and an <em>N</em>-acyliminium ion formation and terminates with a Pictet-Spengler-type aromatic substitution. The method has been used to achieve a rapid and highly effective formal synthesis of erysotramidine.

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18

Lee, Hyoung Ik, Michael P. Cassidy, Paitoon Rashatasakhon, and Albert Padwa. "Efficient Synthesis of (.+-.)-Erysotramidine Using an NBS-Promoted Cyclization Reaction of a Hexahydroindolinone Derivative." ChemInform 35, no. 18 (2004). http://dx.doi.org/10.1002/chin.200418210.

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19

Padwa, Albert, Hyoung Ik Lee, Paitoon Rashatasakhon, and Mickea Rose. "Electrophilic-Induced Cyclization Reaction of Hexahydroindolinone Derivatives and Its Application Toward the Synthesis of (.+-.)-Erysotramidine." ChemInform 36, no. 19 (2005). http://dx.doi.org/10.1002/chin.200519220.

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20

SANO, T., J. TODA, N. KASHIWABA, T. OHSHIMA, and Y. TSUDA. "ChemInform Abstract: Synthesis of Erythrina and Related Alkaloids. Part 16. Diels-Alder Approach: Total Synthesis of d,l-Erysotrine, d,l-Erythraline, d,l-Erysotramidine, d,l-8-Oxoerythraline and Their 3-Epimers." ChemInform 18, no. 34 (1987). http://dx.doi.org/10.1002/chin.198734348.

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