Synthetic studies towards the total synthesis of tedanolide: Formation of the C(13)-C(23) fragment

Teck Peng Loh; Li Chun Feng

doi:10.1016/S0040-4039(01)00401-4

Synthetic studies towards the total synthesis of tedanolide: Formation of the C(13)-C(23) fragment

Teck Peng Loh^*, Li Chun Feng

^*Corresponding author for this work

National University of Singapore

Research output: Contribution to journal › Article › peer-review

46 Citations (Scopus)

Abstract

The C(13)-C(23) subunit of tedanolide was obtained using a boron-mediated aldol reaction as the key step to control the C₁₆ and C₁₇ stereocenters.

Original language	English
Pages (from-to)	3223-3226
Number of pages	4
Journal	Tetrahedron Letters
Volume	42
Issue number	18
DOIs	https://doi.org/10.1016/S0040-4039(01)00401-4
Publication status	Published - Apr 30 2001
Externally published	Yes

ASJC Scopus Subject Areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(01)00401-4

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title = "Synthetic studies towards the total synthesis of tedanolide: Formation of the C(13)-C(23) fragment",

abstract = "The C(13)-C(23) subunit of tedanolide was obtained using a boron-mediated aldol reaction as the key step to control the C16 and C17 stereocenters.",

author = "Loh, \{Teck Peng\} and Feng, \{Li Chun\}",

year = "2001",

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doi = "10.1016/S0040-4039(01)00401-4",

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AU - Loh, Teck Peng

AU - Feng, Li Chun

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Y1 - 2001/4/30

N2 - The C(13)-C(23) subunit of tedanolide was obtained using a boron-mediated aldol reaction as the key step to control the C16 and C17 stereocenters.

AB - The C(13)-C(23) subunit of tedanolide was obtained using a boron-mediated aldol reaction as the key step to control the C16 and C17 stereocenters.

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 18

ER -

Synthetic studies towards the total synthesis of tedanolide: Formation of the C(13)-C(23) fragment

Abstract

ASJC Scopus Subject Areas

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