Photo- and stereochemistry of 5,6-methylenepyrimidine nucleosides, bicylic isomers of thymidine, and 5-methyluridine.

DOI: 10.1021/ja00743a031

Source and publish data:

Journal of the American Chemical Society p. 3478 - 3487 (1971)

Update date:2022-08-04

Topics:

Authors:

Kunieda Kunieda

Witkop Witkop

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

Article abstract of DOI:10.1021/ja00743a031

Full text of DOI:10.1021/ja00743a031

Products guided by the article

Product name:O^{2'_,O3'_{-isopropylidene-3-methyl-O}5'}-trityl-uridine

Cas No:28079-14-3

R&D Labs maybe for 28079-14-3

Changzhou Welton Chemical Co., Ltd,

Contact:0086-519-85910828,85920537,85912897

Address:No.8 Jinlong Road, Binjiang Park, Changzhou, Jiangsu, China.
guide(suzhou) fine materials co. ltd

Contact:0512-80972173

Address:21st Building, No.369 Lushan Rd, New District Suzhou China 215129
Beijing Century Richap Chemistry Co.,Ltd

Contact:+86- 010-64455497

Address:Guannan County, Lianyungang City, Jiangsu Province, China
Chengdu Baishixing Science and Technology Industry Co., Ltd.

website:http://www.cd-bsx.com

Contact:+86-28-88531548

Address:#217,North of Industry Road,Heshan Town,Pujiang County,Chengdu,Sichuan,China.
Shanghai Sungo Technology Chemical Co., Ltd

Contact:0086-21-51385579

Address:Room2010, F/20, Tonghua Plaza, NO 345 Jinxiang Road, Jinqiao Export Processing Zone, Shanghai, 201206 P.R.CHINA

Relevant to this article

A Novel o-Iminophenyl Anion Route to Heterocycles and Ortho-Substituted Anilines

Doi:10.1021/jo00128a040
(1995)
Macrocycle formation by ring-closing metathesis. Application to the syntheses of novel macrocyclic taxoids

Doi:10.1021/ja000293w
(2000)
A strategy for the solution-phase parallel synthesis of N- (pyrrolidinylmethyl)hydroxamic acids

Doi:10.1021/jo000186k
(2000)
Efficient synthesis of novel 3-(het)arylanthranilic acids via a suzuki cross-coupling reaction of 7-iodoisatin with (het)arylboronic acids in water

Doi:10.1021/jo991948i
(2000)
A facile synthesis of functionalized dispirooxindole derivatives via a three-component 1,3-dipolar cycloaddition reaction

Doi:10.3390/molecules18055142
(2013)
Synthesis and evaluation of uterine relaxant activity for a novel series of substituted p-hydroxyphenylethanolamines

Doi:10.1016/j.bmc.2006.06.006
(2006)

Article Doi