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Electronic structure and metal–metal communication in (CpM)2(as-indacene) and (CpM)2(s-indacene) (M = Mn, Fe, Co, Ni) complexes: a DFT investigation. Maria Teresa Garland, Samia Kahlal, Desmond Mac-Leod Carey, Ramiro Arratia-Pérez, Juan Manuel Manríquez, Jean-Yves Saillard , New J. Chem. , 2011 , 35 , 2136

Magnetic resonance energy and topological resonance energy. Jun-ichi Aihara , Phys. Chem. Chem. Phys. , 2016 , 18 , 11847

Synthetical approaches to simple derivatives of as-indacene. R. R. Hill, G. H. Mitchell , Chem. Commun. (London) , 1968 , 314

Chemoenzymatic approaches to the decahydro-as-indacene cores associated with the spinosyn class of insecticide. Martin Banwell, David Hockless, Bevyn Jarrott, Brian Kelly, Andrew Knill, Robert Longmore, Gregory Simpson , J. Chem. Soc., Perkin Trans. 1 , 2000 , 3555

529. Molecular-orbital calculations for some aromatic hydrocarbons. Part I. R. D. Brown , J. Chem. Soc. , 1951 , 2391

A synthesis of (±)-sparteine. Thomas Buttler, Ian Fleming, Sabine Gonsior, Bo-Hye Kim, A.-Young Sung, Hee-Gweon Woo , Org. Biomol. Chem. , 2005 , 3 , 1557

Antiaromatic bisindeno-[n]thienoacenes with small singlet biradical characters: syntheses, structures and chain length dependent physical properties. Xueliang Shi, Paula Mayorga Burrezo, Sangsu Lee, Wenhua Zhang, Bin Zheng, Gaole Dai, Jingjing Chang, Juan T. López Navarrete, Kuo-Wei Huang, Dongho Kim, Juan Casado, Chunyan Chi , Chem. Sci. , 2014 , 5 , 4490

Meldrum’s acid and related compounds in the synthesis of natural products and analogs. Andrey S. Ivanov , Chem. Soc. Rev. , 2008 , 37 , 789

Revisiting indeno[2,1-c]fluorene synthesis while exploring the fully conjugated s-indaceno[2,1-c:6,5-c′]difluorene. Himanshu Sharma, Priyank Kumar Sharma, Soumyajit Das , Chem. Commun. , 2020 , 56 , 11319

Synthesis of the AB ring system of clifednamide utilizing Claisen rearrangement and Diels–Alder reaction as key steps. Inga Loke, Guillaume Bentzinger, Julia Holz, Aruna Raja, Aman Bhasin, Florenz Sasse, Andreas Köhn, Rainer Schobert, Sabine Laschat , Org. Biomol. Chem. , 2016 , 14 , 884