Synthesis of highly substituted dibenzoazocine derivatives by the aza-Claisen rearrangement and intramolecular Heck reaction via 8-exo-trig mode of cyclization

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Abstract

The synthesis of highly substituted dibenzo-azocine systems is still lacking. An efficient synthetic protocol utilizing the sequential aromatic aza-Claisen rearrangement followed by the implementation of the intramolecular Heck reaction as a key step has been developed for the synthesis of various dibenzo-azocine derivatives of biological relevance. © 2009 Elsevier Ltd. All rights reserved.

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Majumdar, K. C., Chattopadhyay, B., & Samanta, S. (2009). Synthesis of highly substituted dibenzoazocine derivatives by the aza-Claisen rearrangement and intramolecular Heck reaction via 8-exo-trig mode of cyclization. Tetrahedron Letters, 50(26), 3178–3181. https://doi.org/10.1016/j.tetlet.2009.01.105

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