Synthetic studies on quassimarin and simalikalactone D: Functionalization of ring C

Qin Jiang; Tony K.M. Shing

doi:10.1016/S0040-4039(01)00964-9

Synthetic studies on quassimarin and simalikalactone D: Functionalization of ring C

Qin Jiang, Tony K.M. Shing

Department of Chemistry

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

6 Citations (Scopus)

Abstract

The tricycle 18 containing the oxygenated ring C is constructed from (S)-carvone in 14 steps involving a Shapiro reaction and a selective acylation as the key steps.

Original language	English
Pages (from-to)	5271-5273
Number of pages	3
Journal	Tetrahedron Letters
Volume	42
Issue number	31
DOIs	https://doi.org/10.1016/S0040-4039(01)00964-9
Publication status	Published - 2001 Jul 30

Keywords

Antitumour compounds
Elimination reactions
Quassinoids

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(01)00964-9

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title = "Synthetic studies on quassimarin and simalikalactone D: Functionalization of ring C",

abstract = "The tricycle 18 containing the oxygenated ring C is constructed from (S)-carvone in 14 steps involving a Shapiro reaction and a selective acylation as the key steps.",

keywords = "Antitumour compounds, Elimination reactions, Quassinoids",

author = "Qin Jiang and Shing, {Tony K.M.}",

year = "2001",

month = jul,

day = "30",

doi = "10.1016/S0040-4039(01)00964-9",

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volume = "42",

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journal = "Tetrahedron Letters",

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T1 - Synthetic studies on quassimarin and simalikalactone D

T2 - Functionalization of ring C

AU - Jiang, Qin

AU - Shing, Tony K.M.

PY - 2001/7/30

Y1 - 2001/7/30

N2 - The tricycle 18 containing the oxygenated ring C is constructed from (S)-carvone in 14 steps involving a Shapiro reaction and a selective acylation as the key steps.

AB - The tricycle 18 containing the oxygenated ring C is constructed from (S)-carvone in 14 steps involving a Shapiro reaction and a selective acylation as the key steps.

KW - Antitumour compounds

KW - Elimination reactions

KW - Quassinoids

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U2 - 10.1016/S0040-4039(01)00964-9

DO - 10.1016/S0040-4039(01)00964-9

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SN - 0040-4039

VL - 42

SP - 5271

EP - 5273

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 31

ER -

Synthetic studies on quassimarin and simalikalactone D: Functionalization of ring C

Abstract

Keywords

ASJC Scopus subject areas

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