Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Enantioselective Synthesis of Tetrahydrocarbazoles through a Michael Addition/Ciamician–Plancher Rearrangement Sequence: Asymmetric Synthesis of a Potent Constrained Analogue of MS‐245
Charles C. J. Loh, Gerhard Raabe, Dieter Enders
Chemistry - A European Journal (2012) Vol. 18, Iss. 42, pp. 13250-13254
Closed Access | Times Cited: 64

Showing 26-50 of 64 citing articles:

Asymmetric synthesis of 3,4-annulated indoles through an organocatalytic cascade approach
Lorenzo Caruana, Mariafrancesca Fochi, Mauro Comes Franchini, et al.
Chemical Communications (2013) Vol. 50, Iss. 4, pp. 445-447
Closed Access | Times Cited: 34
Exploiting the Distal Reactivity of Indolyl Methylenemalononitriles: An Asymmetric Organocatalyzed [4+2] Cycloaddition with Enals Enables the Assembly of Elusive Dihydrocarbazoles
Gloria Rassu, Claudio Curti, Vincenzo Zambrano, et al.
Chemistry - A European Journal (2016) Vol. 22, Iss. 36, pp. 12637-12640
Closed Access | Times Cited: 30
Stereoselective synthesis of highly functionalized tetrahydrocarbazoles through a domino Michael–Henry reaction: an easy access to four contiguous chiral centers
Pradeep Jaiswal, Soumen Biswas, Shivendra Singh, et al.
RSC Advances (2013) Vol. 3, Iss. 27, pp. 10644-10644
Closed Access | Times Cited: 27
An Asymmetric Dehydrogenative Diels–Alder Reaction for the Synthesis of Chiral Tetrahydrocarbazole Derivatives
Xiang Wu, Hai‐Jie Zhu, Shi-Bao Zhao, et al.
Organic Letters (2017) Vol. 20, Iss. 1, pp. 32-35
Closed Access | Times Cited: 27
Asymmetric Synthesis of Tetracyclic Pyrroloindolines and Constrained Tryptamines by a Switchable Cascade Reaction
Corien de Graaff, Lisa Bensch, Sjoerd J. Boersma, et al.
Angewandte Chemie International Edition (2015) Vol. 54, Iss. 47, pp. 14133-14136
Closed Access | Times Cited: 26
Biomimetic Synthesis of Iheyamine A from Spirocyclic Oxindoles
Takumi Abe, Koji Yamada, Syuhei Satake
Heterocycles (2018) Vol. 99, Iss. 1, pp. 379-379
Open Access | Times Cited: 25
Organocatalytic asymmetric synthesis of tetrahydrocarbazoles via an inverse-electron-demand Diels–Alder reaction of 2,3-indole-dienes with enals
Bo‐Qi Gu, Wu‐Lin Yang, Shu‐Xiao Wu, et al.
Organic Chemistry Frontiers (2018) Vol. 5, Iss. 23, pp. 3430-3434
Closed Access | Times Cited: 25
Carbene-Catalyzed Reaction of Indolyl Methylenemalononitriles and Enals for Access to Complex Tetrahydrocarbazoles
Chengli Mou, Liejin Zhou, Runjiang Song, et al.
Organic Letters (2020) Vol. 22, Iss. 7, pp. 2542-2547
Open Access | Times Cited: 22
Ruthenium(II)-Catalyzed Remote C–H Sulfonylation of 2-Pyridones
Fengqi Yang, Pengfei Zhou, Zeng Huang, et al.
Organic Letters (2023) Vol. 25, Iss. 31, pp. 5779-5783
Closed Access | Times Cited: 7
The asymmetric Cu(ii)–indolinylmethanol complex catalyzed Diels–Alder reaction of 2-vinylindoles with β,γ-unsaturated α-ketoesters: an efficient route to functionalized tetrahydrocarbazoles
Banlai Ouyang, Yu Tingting, Renshi Luo, et al.
Organic & Biomolecular Chemistry (2014) Vol. 12, Iss. 24, pp. 4172-4176
Closed Access | Times Cited: 23
The aminoindanol core as a key scaffold in bifunctional organocatalysts
Isaac G. Sonsona, Eugenia Marqués‐López, Raquel P. Herrera
Beilstein Journal of Organic Chemistry (2016) Vol. 12, pp. 505-523
Open Access | Times Cited: 22
Design and Enantioselective Synthesis of β-Vinyl Tryptamine Building Blocks for Construction of Privileged Chiral Indole Scaffolds
Tao‐Yan Lin, Haihong Wu, Jian‐Jun Feng, et al.
ACS Catalysis (2017) Vol. 7, Iss. 6, pp. 4047-4052
Closed Access | Times Cited: 22
Switchable Chemoselectivity for Organocatalytic, Asymmetric Malononitrile Addition to ortho-Formyl Chalcones
Sanjay Maity, Mithu Saha, Gurupada Hazra, et al.
Organic Letters (2017) Vol. 19, Iss. 21, pp. 5872-5875
Closed Access | Times Cited: 22
Potential Rearrangements in the Reaction Catalyzed by the Indole Prenyltransferase FtmPT1
Niusha Mahmoodi, Martin E. Tanner
ChemBioChem (2013) Vol. 14, Iss. 15, pp. 2029-2037
Closed Access | Times Cited: 22
Organocatalytic asymmetric synthesis of dihydrocarbazoles via a formal [4+2] cycloaddition of in situ generated o-quinodimethanes with enals
Bo‐Qi Gu, Hao Zhang, Ruo‐Heng Su, et al.
Tetrahedron (2016) Vol. 72, Iss. 41, pp. 6595-6602
Closed Access | Times Cited: 18
FeCl3-Promoted Annulation of 2-Haloindoles: Switchable Synthesis of Spirooxindole-chromeno[2,3-b]indoles and Spirooxindole-chromeno[3,2-b]indoles
Mupeng Luo, Xinlei Zhu, Rufeng Liu, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 5, pp. 3638-3654
Closed Access | Times Cited: 18
Friedel-Crafts alkylation reaction efficiently catalyzed by a di-amide functionalized Zr(IV) metal-organic framework
Subhrajyoti Ghosh, Nagarathinam Nagarjun, Masud Alam, et al.
Molecular Catalysis (2021) Vol. 517, pp. 112007-112007
Closed Access | Times Cited: 15
Highly Active La(III)‐Based Metal‐Organic Framework as a Heterogeneous Lewis Acid Catalyst for Friedel‐Crafts Alkylation
Jiaqi Wu, Xin‐Yuan Wu, Jian‐Mei Lu, et al.
Chemistry - A European Journal (2022) Vol. 28, Iss. 69
Closed Access | Times Cited: 10
Synthesis of pentacyclic pyrrolo[3,4-a]carbazole-1,3(2H)-diones via an intermolecular Diels–Alder, intramolecular carbonyl-ene reaction strategy
Matokah M. Abualnaja, Paul G. Waddell, W. Clegg, et al.
Tetrahedron (2016) Vol. 72, Iss. 38, pp. 5798-5806
Open Access | Times Cited: 16
Observations arising from a Beckmann rearrangement-Mannich cyclization approach to the azepinobisindole alkaloid iheyamine A
Ashley C. Lindsay, Jonathan Sperry
Tetrahedron (2017) Vol. 73, Iss. 30, pp. 4355-4362
Closed Access | Times Cited: 16
Rapid determination of enantiomeric excess of α-chiral aldehydes using circular dichroism spectroscopy
Sanmitra Barman, Eric V. Anslyn
Tetrahedron (2013) Vol. 70, Iss. 6, pp. 1357-1362
Closed Access | Times Cited: 16
Organocatalytic Asymmetric Synthesis of Trifluoromethylated Tetrahydrocarbazoles by a Vinylogous Michael/Aldol Formal [4+2] Annulation
Ehsan Jafari, Pankaj Chauhan, Mukesh Kumar, et al.
European Journal of Organic Chemistry (2018) Vol. 2018, Iss. 20-21, pp. 2462-2465
Closed Access | Times Cited: 15
Efficiently diastereoselective synthesis of functionalized hydro-carbazoles by base-mediated tandem annulation of 1-(2-amino-aryl)prop-2-en-1-ones and sulfur ylide
Chengyuan Wang, Jiong Zhang, Zheyuan Wang, et al.
Organic Chemistry Frontiers (2020) Vol. 7, Iss. 12, pp. 1469-1473
Closed Access | Times Cited: 14
New syntheses of cycloalka[b]indoles
Р. Р. Гатауллин
Russian Journal of Organic Chemistry (2016) Vol. 52, Iss. 9, pp. 1227-1263
Closed Access | Times Cited: 13
Enantioselective synthesis of functionalised tetrahydrocarbazoles via an organocatalysed Diels–Alder/ene reaction strategy
Joseph Cowell, Ross W. Harrington, Michael R. Probert, et al.
Tetrahedron Asymmetry (2015) Vol. 26, Iss. 20, pp. 1189-1196
Closed Access | Times Cited: 13

Scroll to top