Regioselective synthesis and photooxygenations of furonaphthopyrones starting from 2,7-naphthalenediol

Zhi Fu Tao; Xuhong Qian; Mingcai Fan

doi:10.1016/S0040-4020(97)00845-4

Regioselective synthesis and photooxygenations of furonaphthopyrones starting from 2,7-naphthalenediol

Zhi Fu Tao^*
, Xuhong Qian
, Mingcai Fan

^*Corresponding author for this work

East China University of Science and Technology

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

26 Scopus citations

Abstract

Three angular furonaphthopyrones 4, 9, 12 were regioselectively synthesized starting from 2,7-naphthalenediol in three steps, respectively. An easy separation of Pechmann condensation products 1 and 2 of 2, 7-naphthalenediol with ethyl acetoacetate was described. The photooxygenations of 4, 12 were investigated and a hydroperoxide 18 was isolated and fully characterized.

Original language	English
Pages (from-to)	13329-13338
Number of pages	10
Journal	Tetrahedron
Volume	53
Issue number	39
DOIs	https://doi.org/10.1016/S0040-4020(97)00845-4
State	Published - 29 Sep 1997
Externally published	Yes

Access to Document

10.1016/S0040-4020(97)00845-4

Cite this

@article{a1e2e2c2775946b3b042ff3bee1e41a6,

title = "Regioselective synthesis and photooxygenations of furonaphthopyrones starting from 2,7-naphthalenediol",

abstract = "Three angular furonaphthopyrones 4, 9, 12 were regioselectively synthesized starting from 2,7-naphthalenediol in three steps, respectively. An easy separation of Pechmann condensation products 1 and 2 of 2, 7-naphthalenediol with ethyl acetoacetate was described. The photooxygenations of 4, 12 were investigated and a hydroperoxide 18 was isolated and fully characterized.",

author = "Tao, \{Zhi Fu\} and Xuhong Qian and Mingcai Fan",

year = "1997",

month = sep,

day = "29",

doi = "10.1016/S0040-4020(97)00845-4",

language = "英语",

volume = "53",

pages = "13329--13338",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier Ltd",

number = "39",

}

TY - JOUR

T1 - Regioselective synthesis and photooxygenations of furonaphthopyrones starting from 2,7-naphthalenediol

AU - Tao, Zhi Fu

AU - Qian, Xuhong

AU - Fan, Mingcai

PY - 1997/9/29

Y1 - 1997/9/29

N2 - Three angular furonaphthopyrones 4, 9, 12 were regioselectively synthesized starting from 2,7-naphthalenediol in three steps, respectively. An easy separation of Pechmann condensation products 1 and 2 of 2, 7-naphthalenediol with ethyl acetoacetate was described. The photooxygenations of 4, 12 were investigated and a hydroperoxide 18 was isolated and fully characterized.

AB - Three angular furonaphthopyrones 4, 9, 12 were regioselectively synthesized starting from 2,7-naphthalenediol in three steps, respectively. An easy separation of Pechmann condensation products 1 and 2 of 2, 7-naphthalenediol with ethyl acetoacetate was described. The photooxygenations of 4, 12 were investigated and a hydroperoxide 18 was isolated and fully characterized.

UR - https://www.scopus.com/pages/publications/0030768587

U2 - 10.1016/S0040-4020(97)00845-4

DO - 10.1016/S0040-4020(97)00845-4

M3 - 文章

AN - SCOPUS:0030768587

SN - 0040-4020

VL - 53

SP - 13329

EP - 13338

JO - Tetrahedron

JF - Tetrahedron

IS - 39

ER -

Regioselective synthesis and photooxygenations of furonaphthopyrones starting from 2,7-naphthalenediol

Abstract

Access to Document

Other files and links

Fingerprint

Cite this