𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Total Synthesis of (−)-Neplanocin A by Using Lithium Thiolate-Initiated Michael−Aldol Tandem Cyclization Reaction

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

Book ID
120049280
Publisher
American Chemical Society
Year
2001
Tongue
English
Weight
147 KB
Volume
66
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Total Synthesis of
ChemInform Abstract: Total Synthesis of (-)-Neplanocin A by Using Lithium Thiolate-Initiated Michael—Aldol Tandem Cyclization Reaction.
✍ Masashi Ono; Katsumi Nishimura; Hiroshi Tsubouchi; Yasuo Nagaoka; Kiyoshi Tomiok 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Efficient cyclization of ω-oxo-α,β-unsat
Efficient cyclization of ω-oxo-α,β-unsaturated esters using lithium thiolate-initiated Michael-aldol tandem reaction
✍ Masashi Ono; Katsumi Nishimura; Yasuo Nagaoka; Kiyoshi Tomioka 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 247 KB

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.