陈芬儿

化学

荆门帅邦科技院士工作站

基本信息

陈芬儿（1958.4.7- ）精细有机化工和原料药制造专家。江西崇仁人。1999年毕业于四川大学有机化学专业，获博士学位。现任上海复旦大学化学系教授、博士生导师。长期从事精细有机化工原料药制造技术及工程化研究。发明了氯霉胺类催化剂及配套高立体定向催化醇解技术，在国际上建成了维生素H催化生产新工艺；发明了脂环烃芳香化类的清洁技术，建成了全球产量最大双氯灭痛类系列原料药生产新工艺；建成了均相自催化重排为关键技术洛索洛芬、酮洛芬等原料药通用生产工艺；开发了一系列聚合物氧氮丙啶氧化剂及配套环内酯立体定向氧化技术，建成了世界第一条喜树碱类原料药化学全合成生产线。相关成果获2005年国家技术发明二等奖、2007年国家科技进步二等奖各一项、2006年何梁何利科学与技术进步奖、2006年中国专利金奖及省部级科技一等奖3项。2015年当选为中国工程院院士。

科研成果

总发文数(篇)
0
总被引数(次)
0
H指数
0
篇均被引(次)
0
TOP1%高被引
0
TOP10%高被引
0
FWCI
0
国际合作发文数(篇)
0

成果分析

期刊发文数占比
重点学科匹配度: 论文历年发表情况; 合作发文情况; 文章被引情况

科研论文更多

Studies on anti-inflammatory drugs of 2-arylpropanoic acids: Part IX - A practical synthesis of ketoprofen by 1,2-aryl rearrangement
- 摘要：
  An efficient synthesis of ketoprofen via chloration, Friedel-Crafts ac
- 作者：
  Chen Fener;Liu Jidong;Shao Lanying;Yan Qiongjiao
- 刊名：
  Indian Journal of Chemistry Section B Organic and Medicinal Chemistry
- 在线出版时间：
  1999
Tetrabutylammonium peroxydisulfate in organic synthesis; IX: A convenient approach to the synthesis of fused acetal derivatives by tetrabutylammonium peroxydisulfate-mediated oxidative cycloaddition of 1,3-dicarbonyl compounds to cyclic enol ethers
- 摘要：
  A number of fused acetal derivatives were prepared in 82-90% yield by
- 作者：
  Chen Fen-Er;Fu Han;Meng Ge;Cheng Yu;Hu Ye-Li
- 刊名：
  Synthesis
- 在线出版时间：
  2000
Hypophosphorous acid-iodine: An efficient and mild reagent for cleavage of N-C bond
- 摘要：
  A mixture of hypophosphorous acid (H3PO2) and io
- 作者：
  Meng Ge;He Yan-Ping;Chen Fen-Er
- 刊名：
  Synthetic Communications
- 在线出版时间：
  2003
Synthetic studies on d-biotin. Part 7: A practical asymmetric total synthesis of d-biotin via enantioselective reduction of meso-cyclic imide catalyzed by oxazborolidine
- 摘要：
  A novel and convenient method for the stereoselective synthesis of d-b
- 作者：
  Chen Fen-Er;Dai Hui-Fang;Kuang Yun-Yan;Jia Hui-Qing
- 刊名：
  Tetrahedron Asymmetry
- 在线出版时间：
  2003
Nonnucleoside HIV-1 reverse transcriptase inhibitors: Part I. Synthesis and structure-activity relationship of 1-alkoxymethyl-5-alkyl-6-naphthylmethyl uracils as HEPT analogues
- 摘要：
  1-Alkoxymethyl-5-alkyl-6-naphthylmethyl uracils, which are novel 1-[(2
- 作者：
  Meng Ge;Chen Fen-Er;De Clercq Erik;Balzarini Jan;Pannecouque Christophe
- 刊名：
  Chemical and Pharmaceutical Bulletin
- 在线出版时间：
  2003
Toward total synthesis of yohimbine and reserpine alkaloids; Part 1. An improved synthesis of cis-5, 8-dihydroxy-1, 4, 5, 8, 9, 10-hexahydronaphthalene- 1, 8-lactone via selective reduction of the conjugated ketone with Zn (BH 4 ) 2
- 摘要：
  An improved and high-yielding synthesis of cis-5, 8-dihydroxy-1, 4, 5
- 作者：
  Li Yong Ye;Xu Mei;Chen Fen Er
- 刊名：
  Chinese Chemical Letters
- 在线出版时间：
  2004

科创中国

陈芬儿

基本信息

科研成果

总发文数(篇)

总被引数(次)

H指数

篇均被引(次)

TOP1%高被引

TOP10%高被引

FWCI

国际合作发文数(篇)

成果分析

期刊发文数占比

重点学科匹配度

论文历年发表情况

合作发文情况

文章被引情况

科研论文更多

Studies on anti-inflammatory drugs of 2-arylpropanoic acids: Part IX - A practical synthesis of ketoprofen by 1,2-aryl rearrangement

Tetrabutylammonium peroxydisulfate in organic synthesis; IX: A convenient approach to the synthesis of fused acetal derivatives by tetrabutylammonium peroxydisulfate-mediated oxidative cycloaddition of 1,3-dicarbonyl compounds to cyclic enol ethers

Hypophosphorous acid-iodine: An efficient and mild reagent for cleavage of N-C bond

Synthetic studies on d-biotin. Part 7: A practical asymmetric total synthesis of d-biotin via enantioselective reduction of meso-cyclic imide catalyzed by oxazborolidine

Nonnucleoside HIV-1 reverse transcriptase inhibitors: Part I. Synthesis and structure-activity relationship of 1-alkoxymethyl-5-alkyl-6-naphthylmethyl uracils as HEPT analogues

Toward total synthesis of yohimbine and reserpine alkaloids; Part 1. An improved synthesis of cis-5, 8-dihydroxy-1, 4, 5, 8, 9, 10-hexahydronaphthalene- 1, 8-lactone via selective reduction of the conjugated ketone with Zn (BH 4 ) 2

友情链接

海外专利信息资源系统

省级中心站

科创中国

陈芬儿

基本信息

科研成果

总发文数(篇)

总被引数(次)

H指数

篇均被引(次)

TOP1%高被引

TOP10%高被引

FWCI

国际合作发文数(篇)

成果分析

期刊发文数占比

重点学科匹配度

论文历年发表情况

合作发文情况

文章被引情况

科研论文 更多

Studies on anti-inflammatory drugs of 2-arylpropanoic acids: Part IX - A practical synthesis of ketoprofen by 1,2-aryl rearrangement

Tetrabutylammonium peroxydisulfate in organic synthesis; IX: A convenient approach to the synthesis of fused acetal derivatives by tetrabutylammonium peroxydisulfate-mediated oxidative cycloaddition of 1,3-dicarbonyl compounds to cyclic enol ethers

Hypophosphorous acid-iodine: An efficient and mild reagent for cleavage of N-C bond

Synthetic studies on d-biotin. Part 7: A practical asymmetric total synthesis of d-biotin via enantioselective reduction of meso-cyclic imide catalyzed by oxazborolidine

Nonnucleoside HIV-1 reverse transcriptase inhibitors: Part I. Synthesis and structure-activity relationship of 1-alkoxymethyl-5-alkyl-6-naphthylmethyl uracils as HEPT analogues

Toward total synthesis of yohimbine and reserpine alkaloids; Part 1. An improved synthesis of cis-5, 8-dihydroxy-1, 4, 5, 8, 9, 10-hexahydronaphthalene- 1, 8-lactone via selective reduction of the conjugated ketone with Zn (BH 4 ) 2

友情链接

海外专利信息资源系统

省级中心站

科研论文更多