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Synthesis 2013; 45(17): 2417-2425
DOI: 10.1055/s-0033-1338503
DOI: 10.1055/s-0033-1338503
paper
A Facile and Practical Synthesis of Nicolaou’s Key Intermediates, 2-Methyl- and 2,6-Dimethyltetrahydropyrans, toward the Total Synthesis of Ladder-Shaped Polyethers
Further Information
Publication History
Received: 04 June 2013
Accepted after revision: 13 June 2013
Publication Date:
19 July 2013 (online)
This paper is dedicated to the memory of Choji Ueno.
Abstract
A facile and robust method to prepare 2-methyl- and 2,6-dimethyltetrahydropyrans, most useful Nicolaou intermediates for the synthesis of ladder-shaped polyethers, is disclosed. The established highly practical recipe, adopting chemo- and stereoselective catalytic oxidations and one-pot reactions with few chromatographic purifications, would significantly facilitate the large-scale supply of pivotal monocyclic building blocks, which is a rate-determining process of gigantic tetrahydropyran-containing natural products synthesis.
Key words
total synthesis - ladder-shaped polyethers - trans/syn/trans-fused-ring system - one pot - selective oxidationSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
-
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For the hypothetical, molecular mode of action of LSPs, see:
For perspectives, see:
For reviews on the total synthesis of LSPs, see:
For example, see:
For synthetic studies of yessotoxins, see:
Nicolaou’s intermediates, 1 and/or 2, were used in (a)–(f), (h), and (i).
For synthetic studies of maitotoxin, see:
Nicolaou’s intermediates, 1 and/or 2, were used in (i), (k), (m) and (o).
Shi’s ketone 24 was readily prepared from natural fructose in only two steps; see:
For instance, catalytic IBX or 2-iodoxybenzenesulfonic acid in the presence of Oxone® as a co-oxidant failed to transform alcohol 5 to ketone 12, resulting in the decomposition of the substrate. For details of the catalytic use of IBX-type oxidants with Oxone®, see:
For initial synthetic work with AZADO from an interest in its physical properties as a stable radical, see: