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Synthesis 2020; 52(10): 1576-1584
DOI: 10.1055/s-0039-1691699
DOI: 10.1055/s-0039-1691699
paper
Stereoselective Total Synthesis of Arundinolides A and B
We thank the foundation support from the National Key Research and Development Program of China (2016YFA0203102), the Strategic Priority Research Program of Chinese Academy of Sciences (Grant XDB14040201), National Natural Science Foundation of China (Projects 21302150 and 21602082), Science and Technology Department of Hubei Province (2019CFB596), Chen-Guang program from Hubei Association for Science and Technology, Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University (KLSAOFM1810), Key Laboratory of Hubei Province for Coal Conversion and New Carbon Materials, Wuhan University of Science and Technology (WKDM202003).Weitere Informationen
Publikationsverlauf
Received: 07. Dezember 2019
Accepted after revision: 09. Januar 2020
Publikationsdatum:
05. Februar 2020 (online)
Abstract
The efficient and enantioselective syntheses of arundinolides A and B have been accomplished for the first time from chiral pool methyl-2,3-O-isopropylidene-β-d-ribofuranoside and d-ethyl lactate. The key features of the total synthesis are intramolecular crotonyl migration and NaBH4-CuCl catalyzed regioselective reduction and cross-metathesis reaction.
Key words
arundinolides - total synthesis - chiral pool - regioselective reduction - crotonyl migrationSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0039-1691699.
- Supporting Information
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Isomerization of allylic alcohols to ketones using catalytic or stoichiometric amounts of ruthenium complexes has been reported. For other reports of ethyl ketone formation from allylic alcohols under olefin metathesis reaction using Grubbs reagents, see:
For selected examples of homodimerization suppression by silyl group protection, see: