Facile syntheses of (+)-gabosines A, D, and e

Tony K.M. Shing; Hau M. Cheng

doi:10.1039/b911810a

Facile syntheses of (+)-gabosines A, D, and e

Tony K.M. Shing, Hau M. Cheng

Department of Chemistry

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24 Citations (Scopus)

Abstract

(+)-Gabosines A (12), D (4), and E (5), which share the same trihydroxycyclohexenone skeleton, were synthesized from enone 11 as the common intermediate. The key building block 11 was accessed by an intramolecular aldol cyclization of a diketone derived from d-glucose (8).

Original language	English
Pages (from-to)	5098-5102
Number of pages	5
Journal	Organic and Biomolecular Chemistry
Volume	7
Issue number	24
DOIs	https://doi.org/10.1039/b911810a
Publication status	Published - 2009 Dec 29

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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abstract = "(+)-Gabosines A (12), D (4), and E (5), which share the same trihydroxycyclohexenone skeleton, were synthesized from enone 11 as the common intermediate. The key building block 11 was accessed by an intramolecular aldol cyclization of a diketone derived from d-glucose (8).",

author = "Shing, {Tony K.M.} and Cheng, {Hau M.}",

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PY - 2009/12/29

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N2 - (+)-Gabosines A (12), D (4), and E (5), which share the same trihydroxycyclohexenone skeleton, were synthesized from enone 11 as the common intermediate. The key building block 11 was accessed by an intramolecular aldol cyclization of a diketone derived from d-glucose (8).

AB - (+)-Gabosines A (12), D (4), and E (5), which share the same trihydroxycyclohexenone skeleton, were synthesized from enone 11 as the common intermediate. The key building block 11 was accessed by an intramolecular aldol cyclization of a diketone derived from d-glucose (8).

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JO - Organic and Biomolecular Chemistry

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Facile syntheses of (+)-gabosines A, D, and e

Abstract

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