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- W2996651812 abstract "Abstract We present the first asymmetric total synthesis and absolute configuration determination of (+)‐tronocarpine. The [6.5.7.6.6] pentacyclic core was constructed at an early stage by using a sequential cyclization strategy through a newly developed catalytic asymmetric Michael/aldol cascade to build the aza[3.3.1]‐bridged cycle and a tandem reduction/hemiamidation procedure to assemble the seven‐membered lactam. The side‐chain functionalities were incorporated at a late stage by several appropriately orchestrated manipulations under mild conditions. The synthesis of enantiomerically pure (+)‐tronocarpine was achieved through a 20‐step longest linear sequence from tryptamine." @default.
- W2996651812 created "2019-12-26" @default.
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- W2996651812 date "2020-02-03" @default.
- W2996651812 modified "2023-10-03" @default.
- W2996651812 title "Enantioselective Total Synthesis and Absolute Configuration Assignment of (+)‐Tronocarpine Enabled by an Asymmetric Michael/Aldol Reaction" @default.
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- W2996651812 doi "https://doi.org/10.1002/anie.201914868" @default.
- W2996651812 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31829490" @default.
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