Trans-disubstituted meso-tetraethynylporphyrins

DOI: 10.1016/0040-4039(96)00735-6

Source and publish data:

Tetrahedron Letters p. 4069 - 4072 (1996)

Update date:2022-08-03

Topics:

Authors:

Milgrom, Lionel R.

Yahioglu, Gokhan

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

Article abstract of DOI:10.1016/0040-4039(96)00735-6

Examples of the title porphyrins were prepared (by coupling acetylenic dipyrromethanes with substituted propynals), and their spectroscopic properties reported.

Full text of DOI:10.1016/0040-4039(96)00735-6

Products guided by the article

Product name:meso(phenylethynyl)dipyrromethane

Cas No:178939-83-8

R&D Labs maybe for 178939-83-8

Xi'an Unique Electronic and Chemical Co., Ltd.

Contact:+86-029-88238008

Address:1703# B BUILDING WEST ELECTRONIC ZONE, XI'AN, CHINA
Zhejiang Genebest Pharmaceutical Co.,Ltd.

Contact:0086-571-63532866

Address:No.1 Jinboshi Rd Lishan Town Fuyang City Zhejiang Province China
SICHUAN TONGSHENG AMINOACID CO.LTD

website:http://www.aminoacid.cc

Contact:86-838-2274206/2850606

Address:Room 1-11-1,No.19 of North TianShan Road,Deyang,Sichuan China
Hisyntech Corporation Limited

Contact:0086-22-23410962

Address:17-201, Ningfuli, Shuishanggongyuandong road,Nankai district, Tianjin, China
Dongtai Xinyuan Chemical Co., Ltd.

Contact:+86-21-56733000

Address:404F, 99Nong No.117 Zhongtan Rd. Shanghai

Relevant to this article

Reactions of metallated 1-hydroxy-2,2,4,5,5-pentamethyl-3-imidazoline with electrophiles

Doi:10.1007/BF00699192
(1993)
Lipase-mediated synthesis of enantiopure N-carbobenzoxy-3-hydroxy- 1,2,3,4-tetrahydro- and N-carbobenzoxy-3-hydroxy-1,2,3,6-tetrahydropyridines from 3-hydroxypyridine

Doi:10.1055/s-2000-6363
(2000)
Organocatalytic syntheses of benzoxazoles and benzothiazoles using aryl iodide and oxone via C-H functionalization and C-O/S bond formation

Doi:10.1021/jo501216h
(2014)
Transition-metal-free phenylselenylation of arenes with triflic anhydride activated methyl phenyl selenoxide

Doi:10.1016/j.tetlet.2018.07.005
(2018)
Doi:10.1039/jr9510002177
(1951)
Doi:10.1021/ja01331a045
(1933)

Article Doi