Log in

Relevant bibliographies by topics / Tetrahydropyrrolo[3

Contents

Journal articles

Academic literature on the topic 'Tetrahydropyrrolo[3'

Author: Grafiati

Published: 9 March 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 'Tetrahydropyrrolo[3.'

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 "Tetrahydropyrrolo[3"

1

Konopíková, Marta, Lubor Fišera, and Naďa Prónayová. "Synthesis and Fungicidal Activity of Isoxazolines Fused to 3,5-Dichloromaleimide." Collection of Czechoslovak Chemical Communications 57, no. 7 (1992): 1521–36. http://dx.doi.org/10.1135/cccc19921521.

Full text

Abstract:

3-Phenyl-5-(3,5-dichlorophenyl)-3a,4,6,6a-tetrahydropyrrolo[3,4-d]isoxazoles (III, R = H) and 3-phenyl-5-(3,5-dichlorophenyl)-6a-methyl-3a,4,6,6a-tetrahydropyrrolo[3,4-d]isoxazoles (IV, R = CH3) were prepared by 1,3-dipolar cycloaddition of substituted benzonitrile oxides I to N-(3,5-dichlorophenyl)maleimide (I, R = H), or its methyl derivative II (R = CH3). Cycloaddition to compound II (R = CH3) proceeded regiospecifically. Reduction of IVg with NaBH4 was regio- and stereoselective to yield the hydroxylactams VIIg, VIIIg, and IXg. Antifungal activity of several products was worse than that of

APA, Harvard, Vancouver, ISO, and other styles

2

Yuan, Chunhao, Leijie Zhou, Zhanhu Sun, and Hongchao Guo. "Phosphine-catalyzed [3 + 2] cycloaddition of phthalazinium dicyanomethanides with allenoates: highly efficient synthesis of 1,2,3,10b-tetrahydropyrrolo[2,1-a]phthalazine derivatives." RSC Advances 6, no. 81 (2016): 77931–36. http://dx.doi.org/10.1039/c6ra13643e.

Full text

Abstract:

The phosphine-catalyzed [3 + 2] cycloaddition has been achieved at room temperature, providing novel heterocyclic compounds, 1,2,3,10b-tetrahydropyrrolo[2,1-a]phthalazine derivatives, as single (Z)-isomers in excellent yields (88–99% yield).

APA, Harvard, Vancouver, ISO, and other styles

3

Wang, Bing-Tao, Hua-Dong Yue, Shu-Ping Luo, Li-Ping Wang, and Dan-Qian Xu. "Diphenyl-5,6,7,7a-tetrahydropyrrolo[1,2-c]oxazol-3(1H)-one." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (2007): o1108—o1109. http://dx.doi.org/10.1107/s1600536807004394.

Full text

Abstract:

The title compound, C18H17NO2, synthesized from enantiomerically pure L-proline, methyl chloroformate and a Grignard reagent, crystallizes with two molecules in the asymmetric unit. A chair conformation is adopted by the two fused five-membered rings.

APA, Harvard, Vancouver, ISO, and other styles

4

Barker, David, Lisa Pilkington, Natalie Haverkate, Michelle van Rensburg, Johannes Reynisson, and Euphemia Leung. "Synthesis of 3-Amino-2-carboxamide Tetrahydropyrrolo[2,3-b]quinolines." Synlett 27, no. 20 (2016): 2811–14. http://dx.doi.org/10.1055/s-0036-1588619.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Volovenko, Yulian M., Elizaveta V. Resnyanska, and Anton V. Tverdokhlebov. "A Facile Route to the 6-Hetaryl Substituted Pyrrolo[1,2-a]thieno[3,2-e]pyrimidine Derivatives." Collection of Czechoslovak Chemical Communications 67, no. 3 (2002): 365–72. http://dx.doi.org/10.1135/cccc20020365.

Full text

Abstract:

Hitherto unknown 6-hetaryl-4,5,7,8-tetrahydropyrrolo[1,2-a]thieno[3,2-e]pyrimidine-4,7-diones (7a-7g) were prepared by reaction of ethyl 2-aminothiophene-3-carboxylates 5 with 4-chloro-2-hetaryl-3-oxobutanonitriles 4 in DMF at 100 °C. When the same reagents were treated in the presence of triethylamine, a dependence of the reaction pathway on the nature of the hetaryl substituent in chloronitrile component was observed. This was explained in terms of steric factors.

APA, Harvard, Vancouver, ISO, and other styles

6

Musgrave, RP, NW Jacobsen, G. Bourne, CHL Kennard, G. Smith, and TCW Mak. "Cycloaddition Reactions of 3-Dimethylamino-1-methyl-1,2,4-triazinium-5-olates With Dimethyl Acetylenedicarboxylate." Australian Journal of Chemistry 48, no. 6 (1995): 1175. http://dx.doi.org/10.1071/ch9951175.

Full text

Abstract:

The cycloaddition reactions of some 3-dimethylamino-1-methyl-1,2,4-triazinium-5-olates (1) with dimethyl acetylenedicarboxylate ( dmad ) were studied. The products in all cases were found tobe dimethyl 4-dimethylamino-1-methyl-6-oxo-1,3a,6,6a-tetrahydropyrrolo[3,4-c]pyrazole-3,3a-dicarboxylate derivatives (2). The structure determinations were carried out by 1H and 13C n.m.r. and mass spectrometry, and for one derivative by single-crystal X-ray diffractometry. The mechanism of the reaction is also discussed.

APA, Harvard, Vancouver, ISO, and other styles

7

Elmuradov, Burkhon Zh, Charoskhon E. Makhmadiyarova, Kambarali K. Turgunov, Bakhodir Tashkhodjaev, and Khusnutdin M. Shakhidoyatov. "(4-Nitrophenyl)(1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-yl)methanol monohydrate." Acta Crystallographica Section E Structure Reports Online 67, no. 7 (2011): o1680. http://dx.doi.org/10.1107/s1600536811021775.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Barnes, J. C., J. N. Low, J. D. Paton, A. D. Dunn та K. I. Kinnear. "(Z)-3-(α-Hydroxybenzylidene)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-9-one, C18H14N2O2". Acta Crystallographica Section C Crystal Structure Communications 41, № 2 (1985): 282–84. http://dx.doi.org/10.1107/s0108270185003638.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Omelian, Taras V., Alexey V. Dobrydnev, Oleksandr Yu Utchenko, Eugeniy N. Ostapchuk, Irina S. Konovalova, and Yulian M. Volovenko. "The reactivity of tetrahydropyrrolo[1,2-b]isothiazol-3(2H)-one 1,1-dioxides." Monatshefte für Chemie - Chemical Monthly 151, no. 11 (2020): 1759–72. http://dx.doi.org/10.1007/s00706-020-02694-3.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Bremner, JB, BM Eschler, BW Skelton, and AH White. "Photolysis of Vinylogous Chloroacetamides as a Route to Novel Bridged Heterocycles." Australian Journal of Chemistry 47, no. 10 (1994): 1935. http://dx.doi.org/10.1071/ch9941935.

Full text

Abstract:

Photolysis of 1-( chloroacetyl )-8,9-dimethoxy-2,3,5,6-tetrahydropyrrolo[2,1-a] isoquinoline (4a) and 1-( chloroacetyl )-9,10-dimethoxy-3,4,6,7-tetrahydro-2H-benzo[a] quinolizine (4b) in acidified water/ acetonitrile each gave mixtures of two products: 10,11-dimethoxy-1,4,5,6,7,8-hexahydro-3,6-methano-2H-3-benzazecine-7,13-dione (5) plus crude 7,8-dimethoxy-1,2,4,5,9,10-hexahydrobenzo [de] pyrrolo [3,2,1-ij] isoquinoline-9,10-dione (6); and 12-hydroxy-11-methoxy- 1,2,4,5,6,7,8,9-octahydro-3,7-methano-3-benzazacycloundecine-8,14-dione (7) and 8,9-dimethoxy-2,3,5,6,10,11-hexahydro-1H-benzo[de] p

APA, Harvard, Vancouver, ISO, and other styles

More sources

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!