FeCl3-Catalyzed Highly Diastereoselective Synthesis of Polyhydrobenzo[a]acridinones

Zongkang Wang; Zhengchen Qin; Yajie Yang; Shuxin Jin; Fengyu Bao; Yanzhong Li

doi:10.1002/ajoc.202200009

FeCl₃-Catalyzed Highly Diastereoselective Synthesis of Polyhydrobenzo[a]acridinones

Zongkang Wang, Zhengchen Qin, Yajie Yang, Shuxin Jin, Fengyu Bao, Yanzhong Li

School of Chemistry and Molecular Engineering

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

6 Scopus citations

Abstract

FeCl₃-catalyzed diastereospecific synthesis of tetrahydrobenzo[a]acridin-5(6H)-ones from enaminones was described. Single diastereoisomers were obtained in good to excellent yields. Two C−C bonds and three contiguous stereogenic centers were formed.

Original language	English
Article number	e202200009
Journal	Asian Journal of Organic Chemistry
Volume	11
Issue number	3
DOIs	https://doi.org/10.1002/ajoc.202200009
State	Published - Mar 2022

Keywords

Iron-catalyzed
diastereoselective
enaminones
tetrahydrobenzo[a]acridin-5(6H)-ones

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10.1002/ajoc.202200009

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title = "FeCl3-Catalyzed Highly Diastereoselective Synthesis of Polyhydrobenzo[a]acridinones",

abstract = "FeCl3-catalyzed diastereospecific synthesis of tetrahydrobenzo[a]acridin-5(6H)-ones from enaminones was described. Single diastereoisomers were obtained in good to excellent yields. Two C−C bonds and three contiguous stereogenic centers were formed.",

keywords = "Iron-catalyzed, diastereoselective, enaminones, tetrahydrobenzo[a]acridin-5(6H)-ones",

author = "Zongkang Wang and Zhengchen Qin and Yajie Yang and Shuxin Jin and Fengyu Bao and Yanzhong Li",

note = "Publisher Copyright: {\textcopyright} 2022 Wiley-VCH GmbH",

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doi = "10.1002/ajoc.202200009",

language = "英语",

volume = "11",

journal = "Asian Journal of Organic Chemistry",

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TY - JOUR

T1 - FeCl3-Catalyzed Highly Diastereoselective Synthesis of Polyhydrobenzo[a]acridinones

AU - Wang, Zongkang

AU - Qin, Zhengchen

AU - Yang, Yajie

AU - Jin, Shuxin

AU - Bao, Fengyu

AU - Li, Yanzhong

PY - 2022/3

Y1 - 2022/3

N2 - FeCl3-catalyzed diastereospecific synthesis of tetrahydrobenzo[a]acridin-5(6H)-ones from enaminones was described. Single diastereoisomers were obtained in good to excellent yields. Two C−C bonds and three contiguous stereogenic centers were formed.

AB - FeCl3-catalyzed diastereospecific synthesis of tetrahydrobenzo[a]acridin-5(6H)-ones from enaminones was described. Single diastereoisomers were obtained in good to excellent yields. Two C−C bonds and three contiguous stereogenic centers were formed.

KW - Iron-catalyzed

KW - diastereoselective

KW - enaminones

KW - tetrahydrobenzo[a]acridin-5(6H)-ones

UR - https://www.scopus.com/pages/publications/85124612510

U2 - 10.1002/ajoc.202200009

DO - 10.1002/ajoc.202200009

M3 - 文章

AN - SCOPUS:85124612510

SN - 2193-5807

VL - 11

JO - Asian Journal of Organic Chemistry

JF - Asian Journal of Organic Chemistry

IS - 3

M1 - e202200009

ER -

FeCl₃-Catalyzed Highly Diastereoselective Synthesis of Polyhydrobenzo[a]acridinones

Abstract

Keywords

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