Relevant bibliographies by topics / 1-Azaspirocycles / Journal articles
To see the other types of publications on this topic, follow the link: 1-Azaspirocycles.

Journal articles on the topic '1-Azaspirocycles'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 17 journal articles for your research on the topic '1-Azaspirocycles.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Robinson, Andrea, Zhen Wang, Nicolas Spiccia, Christopher Gartshore, Jayamini Illesinghe, and William Jackson. "A Concise Cross-Metathesis Route to Enantiopure 1-Azaspirocycles." Synthesis 45, no. 22 (2013): 3118–24. http://dx.doi.org/10.1055/s-0033-1338527.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

L. Funk, Raymond, and Joy Umstead Daggett. "Intermolecular Cycloaddition Reactions of Exocyclic Nitrones. Facile Synthesis of 1-Azaspirocycles." HETEROCYCLES 26, no. 8 (1987): 2175. http://dx.doi.org/10.3987/r-1987-08-2175.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Wang, Zhen James, Nicolas Daniel Spiccia, Christopher James Gartshore, Jayamini Illesinghe, William Roy Jackson, and Andrea Jane Robinson. "ChemInform Abstract: A Concise Cross-Metathesis Route to Enantiopure 1-Azaspirocycles." ChemInform 45, no. 15 (2014): no. http://dx.doi.org/10.1002/chin.201415062.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Dake, Gregory. "Recent approaches to the construction of 1-azaspiro[4.5]decanes and related 1-azaspirocycles." Tetrahedron 62, no. 15 (2006): 3467–92. http://dx.doi.org/10.1016/j.tet.2006.01.071.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Ito, Toshimasa, Naoki Yamazaki, and Chihiro Kibayashi. "Synthesis of 1-Azaspirocycles via Lewis Acid-Mediated Spirocyclization of Cyclic N-Acyl-N,O-acetals." Synlett 2001, no. 10 (2001): 1506–10. http://dx.doi.org/10.1055/s-2001-17475.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Ito, Toshimasa, Naoki Yamazaki, and Chihiro Kibayashi. "ChemInform Abstract: Synthesis of 1-Azaspirocycles via Lewis Acid Mediated Spirocyclization of Cyclic N-Acyl-N,O-acetals." ChemInform 33, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.200206152.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Xiao, Kai-Jiong, Jie-Min Luo, Xiao-Er Xia, Yu Wang, and Pei-Qiang Huang. "General One-Pot Reductivegem-Bis-Alkylation of Tertiary Lactams/Amides: Rapid Construction of 1-Azaspirocycles and Formal Total Synthesis of (±)-Cephalotaxine." Chemistry - A European Journal 19, no. 39 (2013): 13075–86. http://dx.doi.org/10.1002/chem.201302096.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Yeh, Ming-Chang P., Cheng-Wei Fang, and Hsin-Hui Lin. "Facile Synthesis of Azaspirocycles via Iron Trichloride-Promoted Cyclization/Chlorination of Cyclic 8-Aryl-5-aza-5-tosyl-2-en-7-yn-1-ols." Organic Letters 14, no. 7 (2012): 1830–33. http://dx.doi.org/10.1021/ol300434m.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Xiao, Kai-Jiong, Jie-Min Luo, Xiao-Er Xia, Yu Wang, and Pei-Qiang Huang. "ChemInform Abstract: General One-Pot Reductive gem-Bis-alkylation of Tertiary Lactams/Amides: Rapid Construction of 1-Azaspirocycles and Formal Total Synthesis of (.+-.)-Cephalotaxine." ChemInform 45, no. 9 (2014): no. http://dx.doi.org/10.1002/chin.201409106.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Yeh, Ming-Chang P., Cheng-Wei Fang, and Hsin-Hui Lin. "ChemInform Abstract: Facile Synthesis of Azaspirocycles via Iron Trichloride Promoted Cyclization/Chlorination of Cyclic 8-Aryl-5-aza-5-tosyl-2-en-7-yn-1-ols." ChemInform 43, no. 31 (2012): no. http://dx.doi.org/10.1002/chin.201231095.

Full text
APA, Harvard, Vancouver, ISO, and other styles
11

Chiba, Shunsuke, and Atsushi Kaga. "Synthesis of Tricyclic Marine Alkaloids, Cylindricines, Lepadiformines, Fasicularin, and Polycitorols: A Recent Update." Synthesis 50, no. 04 (2017): 685–99. http://dx.doi.org/10.1055/s-0036-1589521.

Full text
Abstract:
Cylindricines, lepadiformines, and fasicularin are tricyclic marine alkaloids bearing perhydropyrrolo- and pyrido[2,1-j] frameworks having divergent chemical functionalities. They have been isolated from marine tunicates over the last two decades and found to have a range of cytotoxicity such as DNA-alkylating ability. Recently, polycitorols have emerged as a new member of this alkaloid family. Their unique structural features and biological activities have intrigued many researchers and challenged them in their synthesis. This review describes recent syntheses of the tricyclic alkaloids based
APA, Harvard, Vancouver, ISO, and other styles
12

Kalaitzakis, Dimitris, Eirini Antonatou, and Georgios Vassilikogiannakis. "One-pot synthesis of 1-azaspiro frameworks initiated by photooxidation of simple furans." October 24, 2013. https://doi.org/10.1039/C3CC47690A.

Full text
Abstract:
A range of 1-azaspirocycles, spiroaminals and 1,6-diazaspirocycles has been synthesized, starting from simple and readily accessible furan precursors, using a cascade reaction sequence initiated by singlet oxygen.
APA, Harvard, Vancouver, ISO, and other styles
13

Fleurisson, Claire, Nessrine Graidia, Jihed Azzouz, et al. "Design and Evaluation of Azaspirocycles as RNA binders." Chemistry – A European Journal, November 13, 2024. http://dx.doi.org/10.1002/chem.202403518.

Full text
Abstract:
This study presents efficient synthetic pathways for preparing novel azaspirocycles. These methodologies involve functionalizing key bicyclic hydrazines with a substituent on one of their bridgehead carbon atoms. The desired spirocyclic cores were successfully obtained through double reductive amination reactions, intramolecular cyclizations, and cleavages of the N‐N bond. The isolated molecules possess unique three‐dimensional structures, suggesting potential applications in medicinal chemistry and drug discovery. With the growing interest in targeting nucleic acids as a complementary approac
APA, Harvard, Vancouver, ISO, and other styles
14

Dake, Gregory. "Recent Approaches to the Construction of 1-Azaspiro[4.5]decanes and Related 1-Azaspirocycles." ChemInform 37, no. 27 (2006). http://dx.doi.org/10.1002/chin.200627245.

Full text
APA, Harvard, Vancouver, ISO, and other styles
15

"[4+1]-Spiroannulation of Bromophenols with α,β-Unsaturated Imines: Synthesis of Azaspirocycles". Synfacts 16, № 12 (2020): 1404. http://dx.doi.org/10.1055/s-0040-1719477.

Full text
APA, Harvard, Vancouver, ISO, and other styles
16

FUNK, R. L., and J. UMSTEAD DAGGETT. "ChemInform Abstract: Intermolecular Cycloaddition Reactions of Exocyclic Nitrones. Facile Synthesis of 1-Azaspirocycles." ChemInform 19, no. 4 (1988). http://dx.doi.org/10.1002/chin.198804218.

Full text
APA, Harvard, Vancouver, ISO, and other styles
17

BRYCE, M. R., J. M. GARDINER, P. J. HORTON, and S. A. SMITH. "ChemInform Abstract: Synthesis and Reactions of 1-Azaspirocycles: 1-Azaspiro(4.5)decane and 1-Azaspiro(4.4)nonane Ring Systems." ChemInform 20, no. 27 (1989). http://dx.doi.org/10.1002/chin.198927161.

Full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography