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- Synthetic studies towards putative yuremamine using an iterative C(sp3)–H arylation strategy. Matthew B. Calvert, Jonathan Sperry
, Org. Biomol. Chem.
, 2016
, 14
, 5728
- Bioinspired total synthesis and structural revision of yuremamine, an alkaloid from the entheogenic plant Mimosa tenuiflora. Matthew B. Calvert, Jonathan Sperry
, Chem. Commun.
, 2015
, 51
, 6202
- Cu(OTf)2 catalysed [6+2] cycloaddition reaction for the synthesis of highly substituted pyrrolo[1,2-a]indoles: rapid construction of the yuremamine core. Dattatraya H. Dethe, Raghavender Boda, Saikat Das
, Chem. Commun.
, 2013
, 49
, 3260
- [3 + 2] Annulations between indoles and α,β-unsaturated ketones: access to pyrrolo[1,2-a]indoles and model reactions toward the originally assigned structure of yuremamine. Haokun Li, Zhonglei Wang, Liansuo Zu
, RSC Adv.
, 2015
, 5
, 60962
- The importance of asking “how and why?” in natural product structure elucidation. Patrick D. Brown, Andrew L. Lawrence
, Nat. Prod. Rep.
, 2017
, 34
, 1193
- The rapid construction and biological evaluation of densely substituted pyrrolo[1,2-a]indoles via a BF3·OEt2-assisted cascade approach. Ghanshyam Mali, Vinay Kumar Yadav, Himani Priya, Manjari Shukla, Peeyush Pandey, Akhilesh Kumar, Manikandan Paranjothy, Sudipta Bhattacharyya, Rohan D. Erande
, Org. Biomol. Chem.
, 2023
, 21
, 9659
- Diastereoselective palladium-catalyzed functionalization of prochiral C(sp3)–H bonds of aliphatic and alicyclic compounds. Srinivasarao Arulananda Babu, Yashika Aggarwal, Pooja Patel, Radha Tomar
, Chem. Commun.
, 2022
, 58
, 2612
- Recent advances in the synthesis of pyrrolo[1,2-a]indoles and their derivatives. Yogesh G. Shelke, Pankaj E. Hande, Santosh J. Gharpure
, Org. Biomol. Chem.
, 2021
, 19
, 7544
- Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles. Kai Chen, Zhen Zhang, Yin Wei, Min Shi
, Chem. Commun.
, 2012
, 48
, 7696
- Enantioselective hydroacylation of N-vinylindole-2-carboxaldehydes. Avipsa Ghosh, Levi M. Stanley
, Chem. Commun.
, 2014
, 50
, 2765