The Reactions of 2-Phenyl-2H-1-benzopyrans and 2-Phenyl-4H-1-benzopyrans with Lead(IV) Acetate

DOI: 10.1246/bcsj.53.1769

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1769 - 1770 (1980)

Update date:2022-08-04

Topics:

Authors:

Kurosawa, Kazu

Yamaguchi, Katsutoshi

Nagata, Yasuyuki

Ohki, Hisatake

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1246/bcsj.53.1769

The reactions of 7-methoxy-2-phenyl-2H-1-benzopyran and 7-methoxy-2-phenyl-4H-1-benzopyran with lead(IV) acetate gave 2-benzoyl-6-methoxybenzofuran and 6-acetoxy-3-methoxy-6-(3-oxo-3-phenyl-1-propenyl)-2,4-cyclohexadien-1-one.The reactions of 7-methoxy-2-

Full text of DOI:10.1246/bcsj.53.1769

Products guided by the article

Product name:6-acetoxy-3-methoxy-6-(3-oxo-3-phenyl-1-propenyl)-2,4-cyclohexadien-1-one

Cas No:75158-61-1

R&D Labs maybe for 75158-61-1

Shanghai Minstar Chemical Co., Ltd

website:http://www.minstargroup.com

Contact:86-21-18019205509

Address:BUILDING 8, NO.1098, CHUANSHA ROAD, SHANGHAI, CHINA
Shanghai PotentPharm Science and Technology Co.,Ltd

Contact:86-021-51969655

Address:Unit B, Building 18, No.300, Chuantu Rd,Pudong District, Shanghai 201202, China
Hubei Vanz Pharm Co.,Ltd

website:http://www.vanzpharm.com/en/index.html

Contact:86-27-84492310

Address:FANHU INDUSTRY PARK
Zhejiang Linhai Xinhua Chemicals Factory

Contact:0086-13661858911

Address:Xunqiao Development Zone, Linhai, Zhejiang, China
Shanghai Yuanye Bio-Technology Co., Ltd.

website:http://www.shyuanye.com

Contact:+86-21-61845781

Address:Building 6, No. 465, Changta Road,Songjiang District,Shanghai,China

Relevant to this article

Synthesis and structure-activity correlations of the cytotoxic bifunctional 1,4-diamidoanthraquinone derivatives

Doi:10.1016/j.bmc.2004.09.001
(2004)
Nucleophilic Reactions of Hexafluoro-1,2-epoxypropane with 1,2-Bifunctional Ethanes

Doi:10.1246/bcsj.53.1694
(1980)
Regioselective Ring Opening in Substituted Benzocyclopropenes. An Alternative or Complementary Mechanism for Electrophilic Substitution Involving Attack at a ? Bond

Doi:10.1021/ja00543a032
(1980)
Infrared Frequency-Modulation Probing of Product Formation in Alkyl + O₂ Reactions: I. the Reaction of C₂H₅ with O₂ between 295 and 698 K

Doi:10.1021/jp0024874
(2000)
Total Synthesis of Echinoside A, a Representative Triterpene Glycoside of Sea Cucumbers

Doi:10.1002/anie.201703610
(2017)
Doi:10.1021/ja01098a512
(1953)

Article Doi