The first stereoselective total synthesis of lankanolide. Part 1: Computer-assisted design and lactonization of model seco-acid derivatives-Reference-Cited by-同舟云学术

The first stereoselective total synthesis of lankanolide. Part 1: Computer-assisted design and lactonization of model seco-acid derivatives

Published:2003-06 Issue:23 Volume:44 Page:4343-4346
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Hamada Tatsuo,Kobayashi Yukinari,Kiyokawa Mitsugu,Yonemitsu Osamu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

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2. Stoffwechselprodukte von Mikroorganismen. 103. Mitteilung [1]. Zur Stereochemie des Lankamycins

3. Fragment synthesis: (a) Kotchetkov, N. K.; Yashunsky, D. V.; Sviridov, A. F.; Ermenko, M. S. Carbohydr. Res. 1990, 200, 209; (b) Raimundo, B. C.; Heathcock, C. H. Synlett 1995, 1213; (c) Paterson, I. Tetrahedron Lett. 1983, 24, 1311.

4. Total synthesis of 16-membered tetraene macrolide hygrolidin

5. Goto, H.; Osawa, E. J. Chem. Soc., Perkin Trans. 2 1993, 187. We used the latest version 4.02 of conflex working on pc-unix (linux) and using extended MM2 as a force field.

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