A straightforward and efficient synthetic access to biologically active marine sesterterpenoids, sesterstatins 4 and 5

Wen-Yuan Fan; Zheng-Lin Wang; Hong-Chang Li; John S Fossey; Wei-Ping Deng

doi:10.1039/c0cc04857g

A straightforward and efficient synthetic access to biologically active marine sesterterpenoids, sesterstatins 4 and 5

Wen-Yuan Fan, Zheng-Lin Wang, Hong-Chang Li, John S Fossey, Wei-Ping Deng

Chemistry

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

16 Citations (Scopus)

Abstract

A straightforward and efficient synthesis of sesterstatins 4 and 5 is reported, in which the reductive Heck cyclisation was employed as the key step for constructing the D ring.

Original language	English
Pages (from-to)	2961-3
Number of pages	3
Journal	Chemical Communications
Volume	47
Issue number	10
Early online date	17 Jan 2011
DOIs	https://doi.org/10.1039/c0cc04857g
Publication status	Published - 14 Mar 2011

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title = "A straightforward and efficient synthetic access to biologically active marine sesterterpenoids, sesterstatins 4 and 5",

abstract = "A straightforward and efficient synthesis of sesterstatins 4 and 5 is reported, in which the reductive Heck cyclisation was employed as the key step for constructing the D ring.",

author = "Wen-Yuan Fan and Zheng-Lin Wang and Hong-Chang Li and Fossey, {John S} and Wei-Ping Deng",

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AU - Fan, Wen-Yuan

AU - Wang, Zheng-Lin

AU - Li, Hong-Chang

AU - Fossey, John S

AU - Deng, Wei-Ping

PY - 2011/3/14

Y1 - 2011/3/14

N2 - A straightforward and efficient synthesis of sesterstatins 4 and 5 is reported, in which the reductive Heck cyclisation was employed as the key step for constructing the D ring.

AB - A straightforward and efficient synthesis of sesterstatins 4 and 5 is reported, in which the reductive Heck cyclisation was employed as the key step for constructing the D ring.

U2 - 10.1039/c0cc04857g

DO - 10.1039/c0cc04857g

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SN - 1364-548X

VL - 47

SP - 2961

EP - 2963

JO - Chemical Communications

JF - Chemical Communications

IS - 10

ER -

A straightforward and efficient synthetic access to biologically active marine sesterterpenoids, sesterstatins 4 and 5

Abstract

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