| Literature DB >> 23731121 |
Matthew G LaPorte1, Sammi Tsegay, Ki Bum Hong, Chunliang Lu, Cheng Fang, Lirong Wang, Xiang-Qun Xie, Paul E Floreancig.
Abstract
A library of spirooxindoles containing varied elements of structural and stereochemical diversity has been constructed via a three step, one pot nitrile hydrozirconation-acylation-cyclization reaction sequence from common acyclic indole intermediates. The resulting library was evaluated for novelty through comparison with MLSMR and Maybridge compound collections.Entities:
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Year: 2013 PMID: 23731121 PMCID: PMC3800499 DOI: 10.1021/co4000387
Source DB: PubMed Journal: ACS Comb Sci ISSN: 2156-8944 Impact factor: 3.784