Relevant bibliographies by topics / N-acylpyrroles

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'N-acylpyrroles'

Author: Grafiati
Published: 20 February 2023
Last updated: 31 July 2025

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

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'N-acylpyrroles.'

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.

Journal articles on the topic "N-acylpyrroles"

1

Duan, Jian-Hua, Rui-Jie Mi, Jing Sun, and Ming-Dong Zhou. "Regioselective C5 alkenylation of 2-acylpyrroles via Pd(ii)-catalyzed C–H bond activation." Organic Chemistry Frontiers 5, no. 2 (2018): 162–65. http://dx.doi.org/10.1039/c7qo00732a.

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

Goldys, Anna M., and Christopher S. P. McErlean. "N-Acylpyrroles: More Than Amides." European Journal of Organic Chemistry 2012, no. 10 (2011): 1877–88. http://dx.doi.org/10.1002/ejoc.201101470.

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

Chen, Weiqiang, Yin-Lin Zhang, Hui-Jing Li, Xiang Nan, Ying Liu, and Yan-Chao Wu. "Synthesis of N-Sulfonyl- and N-Acylpyrroles via a Ring-Closing Metathesis/Dehydrogenation Tandem Reaction." Synthesis 51, no. 19 (2019): 3651–66. http://dx.doi.org/10.1055/s-0039-1690002.

Full text
Abstract:
N-Sulfonyl- and N-acylpyrroles were synthesized via olefin ring-closing metathesis of diallylamines and in situ oxidative aromatization in the presence of the ruthenium Grubbs catalyst and a suitable copper catalyst. In the presence of Cu(OTf)2 and CuBr2, the reaction afforded N-sulfonyl- and N-acylpyrroles, respectively, in one pot. Under an oxygen atmosphere, the reaction went smoothly without the need of hydroperoxide oxidants. This protocol possesses many advantages, such as using a nonhazardous oxidant and readily available starting materials, operating in one pot, and showing a broad sub
APA, Harvard, Vancouver, ISO, and other styles
4

Goldys, Anna M., and Christopher S. P. McErlean. "ChemInform Abstract: N-Acylpyrroles: More Than Amides." ChemInform 43, no. 30 (2012): no. http://dx.doi.org/10.1002/chin.201230235.

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

D’Silva, Claudius, and Rifat Iqbal. "A New Method to N-Arylmethylenepyrroles from N-Acylpyrroles." Synthesis 1996, no. 04 (1996): 457–58. http://dx.doi.org/10.1055/s-1996-4247.

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

Cui, Hai-Lei, and Fujie Tanaka. "One-pot synthesis of polysubstituted 3-acylpyrroles by cooperative catalysis." Org. Biomol. Chem. 12, no. 31 (2014): 5822–26. http://dx.doi.org/10.1039/c4ob01019a.

Full text
Abstract:
Polysubstituted 3-acylpyrroles were synthesized from readily available unsaturated ketones and N-substituted propargylated amines via an aza-Michael/alkyne carbocyclization cascade followed by oxidation in one pot.
APA, Harvard, Vancouver, ISO, and other styles
7

D'SILVA, C., and R. IQBAL. "ChemInform Abstract: A New Method to N-Arylmethylenepyrroles from N-Acylpyrroles." ChemInform 27, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199636112.

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

X., J. Shi, K. Su W., and G. Shan W. "Vilsmeier-Haack preparation of 2-acylpyrroles using bis( trichloromethyl)carbonate and N,N -dimethylacylamines." Journal of Indian Chemical Society Vol. 82, Nov 2005 (2005): 1019–21. https://doi.org/10.5281/zenodo.5825042.

Full text
Abstract:
College of Pharmaceutical Sciences, Zhejiang University of Technology. Hangzhou, 310014, P. R. China <em>E-mail</em>: suweike@zjut.edu.cn&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;<em>Fax</em> : 86-571-88320752 <em>Manuscript received 14 February 2005, revised 28 May 2005, accepted 18 July 2005</em> A series of 2-acylpyrroles were synthesized by using bis(trichloromethyl)carbonate and <em>N,N</em>-dimethylacylamines as Vilsmeier-Haack reagents under mild conditions in good yields.
APA, Harvard, Vancouver, ISO, and other styles
9

Brandänge, Svante, Benito Rodriguez, Nils Gunnar Johansson, and Ann-Britt Wassgren. "N-Acylpyrroles as Acylating Agents. Synthesis of beta-Keto Esters." Acta Chemica Scandinavica 41b (1987): 740–44. http://dx.doi.org/10.3891/acta.chem.scand.41b-0740.

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

Yang, Fan, Dong Zou, Shuguang Chen, et al. "Transition Metal‐Free Aroylation of Diarylmethanes with N ‐Bn‐ N ‐Boc Arylamides and N ‐Acylpyrroles." Advanced Synthesis & Catalysis 362, no. 16 (2020): 3423–30. http://dx.doi.org/10.1002/adsc.202000622.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "N-acylpyrroles"

1

Phippen, Christopher. "Studies Toward the Total Synthesis of Hinckdentine A using Under Utilised Reactions and Functional Groups." Thesis, The University of Sydney, 2014. http://hdl.handle.net/2123/11522.

Full text
Abstract:
Many useful organic transformations remain underutilised because they have not been thoroughly investigated and understood. We have sought to expand the utility of neglected reactions and functional groups by investigating their mechanism and examining their scope. We planned to demonstrate utility of these transformations by incorporating them as key steps in the total synthesis of the natural product hinckdentine A. We developed a rational and consistent theory for mechanism of on-water catalysis. This new theory has allowed us to identify previously unrecognised examples of this phenome
APA, Harvard, Vancouver, ISO, and other styles
2

Holden, Wendy G. "Part I. 2+2 photocycloaddition reactions of N-acylpyrroles with alkenes. Part II. Photochemical reactions of indoles with nucleophiles." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0014/NQ42529.pdf.

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

Book chapters on the topic "N-acylpyrroles"

1

Taber, Douglass F. "Enantioselective Construction of Alkylated Centers: The Maier Synthesis of Platencin." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0039.

Full text
Abstract:
Jaesook Yun of Sungkyunkwan University devised (J. Org. Chem. 2009, 74, 4232) a method, based on conjugate addition to a cyano alkyne, for the preparation of nitriles such as 1 with high geometric control. Enantioselective conjugate reduction then delivered the doubly arylated stereogenic center of 2 in high ee. Pher G. Andersson of Uppsala University described (J. Am. Chem. Soc. 2009, 131, 8855) a similar approach to diarylated ternary stereogenic centers. Motomu Kanai and Masakatsu Shibasaki of the University of Tokyo developed (J. Am. Chem. Soc. 2009, 131, 3858) a complementary approach to
APA, Harvard, Vancouver, ISO, and other styles
2

Lambert, Tristan H. "Construction of Stereochemical Arrays." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0045.

Full text
Abstract:
The unprecedented enantioselective 1,8-addition of azlactone 1 to acylpyrrole 2 catalyzed by triaminophosphorane 3 was reported (J. Am. Chem. Soc. 2012, 134, 19370) by Takashi Ooi at Nagoya University. Tomislav Rovis at Colorado State University developed (Angew. Chem. Int. Ed. 2012, 51, 12330) the asymmetric oxidative hetero-Diels-Alder reaction of propionaldehyde (5) and ketone 6 to produce lactone 8, catalyzed by NHC catalyst 7 in the presence of phenazine. A related NHC catalyst 11 was utilized (Angew. Chem. Int. Ed. 2012, 51, 8276) by Xue-Wei Liu at Nanyang Technological University for th
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'N-acylpyrroles' for particular source types:
Journal articles
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