Highly diastereoselective titanium tetrachloride-mediated aldol condensation of the bistrimethylsilyl enol ether of acetoacetic ester with 2-benzyloxyhexanal. A synthesis of (

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Highly diastereoselective titanium tetrachloride-mediated aldol condensation of the bistrimethylsilyl enol ether of acetoacetic ester with 2-benzyloxyhexanal. A synthesis of (–)-pestalotin

Published:1986 Issue:11 Volume: Page:860-861
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Hagiwara Hisahiro,Kimura Katsuhiko,Uda Hisashi

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1986/C3/C39860000860

Cited by 36 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Divergent Asymmetric Total Synthesis of All Four Pestalotin Diastereomers from (R)-Glycidol;Molecules;2020-01-17

2. The Asymmetric Vinylogous Mukaiyama Aldol Reaction;Organic Reactions;2019-03-11

3. A rapid and diverse construction of 6-substituted-5,6-dihydro-4-hydroxy-2-pyrones through double Reformatsky reaction;Tetrahedron;2013-12

4. Aldol Reaction-Homogeneous;Encyclopedia of Catalysis;2011-02-15

5. Practical and robust method for stereoselective preparations of ketene silyl (thio)acetal derivatives and NaOH-catalyzed crossed-Claisen condensation between ketene silyl acetals and methyl esters;Tetrahedron;2009-07

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