Solvent-free Ugi four-component condensation: application to synthesis of philanthotoxins-12 analogues

Nianjin Liu; Song Cao; Jingjing Wu; Jinlong Yu; Li Shen; Xin Feng; Xuhong Qian

doi:10.1016/j.tet.2008.02.051

Solvent-free Ugi four-component condensation: application to synthesis of philanthotoxins-12 analogues

Nianjin Liu, Song Cao^*, Jingjing Wu, Jinlong Yu, Li Shen, Xin Feng, Xuhong Qian

^*Corresponding author for this work

East China University of Science and Technology

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

22 Scopus citations

Abstract

Philanthotoxins-12 analogues was synthesized by a highly convergent approach, utilizing an efficient, simple, and convenient one-pot Ugi four-component solvent-free method as key step, followed by removal of the protecting groups in the presence of trifluoroacetic acid.

Original language	English
Pages (from-to)	3966-3974
Number of pages	9
Journal	Tetrahedron
Volume	64
Issue number	18
DOIs	https://doi.org/10.1016/j.tet.2008.02.051
State	Published - 28 Apr 2008
Externally published	Yes

Keywords

Philanthotoxins analogues
Solvent-free
Ugi 4CR
α-Acylamino amide

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10.1016/j.tet.2008.02.051

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title = "Solvent-free Ugi four-component condensation: application to synthesis of philanthotoxins-12 analogues",

abstract = "Philanthotoxins-12 analogues was synthesized by a highly convergent approach, utilizing an efficient, simple, and convenient one-pot Ugi four-component solvent-free method as key step, followed by removal of the protecting groups in the presence of trifluoroacetic acid.",

keywords = "Philanthotoxins analogues, Solvent-free, Ugi 4CR, α-Acylamino amide",

author = "Nianjin Liu and Song Cao and Jingjing Wu and Jinlong Yu and Li Shen and Xin Feng and Xuhong Qian",

year = "2008",

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doi = "10.1016/j.tet.2008.02.051",

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T1 - Solvent-free Ugi four-component condensation

T2 - application to synthesis of philanthotoxins-12 analogues

AU - Liu, Nianjin

AU - Cao, Song

AU - Wu, Jingjing

AU - Yu, Jinlong

AU - Shen, Li

AU - Feng, Xin

AU - Qian, Xuhong

PY - 2008/4/28

Y1 - 2008/4/28

N2 - Philanthotoxins-12 analogues was synthesized by a highly convergent approach, utilizing an efficient, simple, and convenient one-pot Ugi four-component solvent-free method as key step, followed by removal of the protecting groups in the presence of trifluoroacetic acid.

AB - Philanthotoxins-12 analogues was synthesized by a highly convergent approach, utilizing an efficient, simple, and convenient one-pot Ugi four-component solvent-free method as key step, followed by removal of the protecting groups in the presence of trifluoroacetic acid.

KW - Philanthotoxins analogues

KW - Solvent-free

KW - Ugi 4CR

KW - α-Acylamino amide

UR - https://www.scopus.com/pages/publications/40849097420

U2 - 10.1016/j.tet.2008.02.051

DO - 10.1016/j.tet.2008.02.051

M3 - 文章

AN - SCOPUS:40849097420

SN - 0040-4020

VL - 64

SP - 3966

EP - 3974

JO - Tetrahedron

JF - Tetrahedron

IS - 18

ER -

Solvent-free Ugi four-component condensation: application to synthesis of philanthotoxins-12 analogues

Abstract

Keywords

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