Abstract
The natural product balanol has served as a template for the design and synthesis of a combinatorial library using solid-phase chemistry. Using a retrosynthetic analysis, the structural analogues have been assembled from three relatively accessible building blocks. The solid-phase chemistry including MSNT-mediated esterification of both support-bound alcohols and carboxylic acids has been implemented successfully. Copyright (C) 1996 Elsevier Science Ltd.
Original language | English |
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Journal | Tetrahedron Letters |
Volume | 37 |
Issue number | 46 |
Pages (from-to) | 8439-8442 |
ISSN | 0040-4039 |
DOIs | |
Publication status | Published - 1996 |