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Efficient cyclization of ω-oxo-α,β-unsaturated esters using lithium thiolate-initiated Michael-aldol tandem reaction

✍ Scribed by Masashi Ono; Katsumi Nishimura; Yasuo Nagaoka; Kiyoshi Tomioka


Book ID
104262221
Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
247 KB
Volume
40
Category
Article
ISSN
0040-4039

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✦ Synopsis


The reaction of to-oxo-(x,13-unsaturated esters with lithium thiolates afforded the Michael-aldol tandem cyclization products in good to perfect stereoselectivity depending on the nature of thiolates.


📜 SIMILAR VOLUMES


Asymmetric Michael–aldol tandem cyclizat
✍ Katsumi Nishimura; Hiroshi Tsubouchi; Masashi Ono; Tomoharu Hayama; Yasuo Nagaok 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 111 KB

The asymmetric reaction of v-oxo-a,b-unsaturated esters with lithium chiral thiolates afforded the Michael-aldol tandem cyclization products in high yield and good stereoselectivity. Reductive desulfurization gave the corresponding optically pure 2-hydroxycycloalkanecarboxylates.

ChemInform Abstract: Total Synthesis of
✍ Masashi Ono; Katsumi Nishimura; Hiroshi Tsubouchi; Yasuo Nagaoka; Kiyoshi Tomiok 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

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