@article{a94a136c735c4995a54f88c84e138066,
title = "Recent development of vinylogous Mukaiyama aldol reactions",
abstract = "The vinylogous Mukaiyama aldol reaction (VMAR) is a powerful tool of polyketide synthesis, which constructs a large size structure by simultaneous introduction of the stereogenic center(s) and the α,β-unsaturated carbonyl group. A variety of stereocontrolled VMARs have been developed and applied to natural product synthesis. This review is focused on recent development of the vinylogous Mukaiyama aldol reaction using s-trans silyl dienolates.",
keywords = "Natural product synthesis, Polyketide, Silyl dienolate, Stereoselective synthesis, Vinylogous Mukaiyama aldol reaction",
author = "Seijiro Hosokawa",
note = "Funding Information: Authors are grateful for financial support to The NOVARTIS Foundation (Japan) for the Promotion of Science, The Kurata Memorial Hitachi Science and Technology Foundation, The Naito Foundation, The Sumitomo Foundation, and MEXT, Japan. Funding Information: Authors are grateful for financial support to The NOVARTIS Foundation (Japan) for the Promotion of Science, The Kurata Memorial Hitachi Science and Technology Foundation , The Naito Foundation , The Sumitomo Foundation , and MEXT , Japan. Publisher Copyright: {\textcopyright} 2017 Elsevier Ltd",
year = "2018",
month = jan,
day = "10",
doi = "10.1016/j.tetlet.2017.11.056",
language = "English",
volume = "59",
pages = "77--88",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "2",
}