November 14, 2001Organic Letters

Efficient Strategy for the Synthesis of Stereopentad Subunits of Scytophycin, Rifamycin S, and Discodermolide

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Abstract

[reaction: see text] An efficient, simple method has been developed for the stereocontrolled synthesis of polypropionate stereopentads in high enantio- and diastereomeric purities.

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BouzBouz et al. (2001) studied this question.

synapsesocial.com/papers/6a9378f83eb9fa3bd61caba5 https://doi.org/10.1021/ol016250h

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Abstract

[reaction: see text] An efficient, simple method has been developed for the stereocontrolled synthesis of polypropionate stereopentads in high enantio- and diastereomeric purities.

Efficient Strategy for the Synthesis of Stereopentad Subunits of Scytophycin, Rifamycin S, and Discodermolide

Abstract

Discussion

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Efficient Strategy for the Synthesis of Stereopentad Subunits of Scytophycin, Rifamycin S, and Discodermolide

Abstract

Discussion

Cite This Study

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