Oxidation of uracil derivatives and pyrimidine nucleosides by dimethyldioxirane: A new and mild synthesis of 5,6-oxiranyl-5,6-dihydro and 5,6-dihydroxy-5,6-dihydro-derivatives

DOI: 10.1016/S0040-4039(00)73740-3

Source and publish data:

Tetrahedron Letters p. 6313 - 6316 (1993)

Update date:2022-08-03

Topics:

Authors:

Lupattelli, Paolo

Saladino, Raffaele

Mincione, Enrico

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

Article abstract of DOI:10.1016/S0040-4039(00)73740-3

The oxidation of title substrates with dimethyldioxirane afforded 5,6-oxiranyl-5,6-dihydro and cis- / trans-5,6-disubstituted-5,6-dihydro-derivatives.

Full text of DOI:10.1016/S0040-4039(00)73740-3

Products guided by the article

Product name:tras-1,3,5-trimethyl-5,6-dihydroxy-5,6-dihydro uracil

Cas No:92207-39-1

R&D Labs maybe for 92207-39-1

NINGBO PANGS CHEM INT’L CO.,LTD.

Contact:+86-574-27666845

Address:FLOOR 21,BUILDING NO.11,XIN TIAN DI,NO.689 SHI JI ROAD,NINGBO CHINA
WUHU HUAHAI BIOLOGY ENGINEERING CO LTD

Contact:+86-553-3836920

Address:7/F NO.82 LAODONG ROAD WUHU CHINA
Shanghai HengXun Pharmaceutical Tech. Co., Ltd.

Contact:86-86-52730756

Address:Room 603, No. 240, Tianmuzhong Road, Zhabei, Shanghai, China
Shandong Xiangde Biotechnology Co., Ltd

Contact:+86 -15066639877

Address:Sanba street
ANGCHEN BRIGHTCHEM CO., LTD

website:http://www.angchenchem.com

Contact:+86-510-88302099 82327577

Address:Rm. 404/405, Floor 4th, No. 983 FengXiang Road, Wuxi, China

Relevant to this article

Iodine-Mediated Synthesis of Aromatic Thioethers with Aromatic Amines and Sulfonyl Hydrazides in High Regioselectivity via C(sp²)-H Bond Functionalization

Doi:10.1002/adsc.201500943
(2016)
Electro-oxidative C(sp²)-H/O-H cross-dehydrogenative coupling of phenols and tertiary anilines for diaryl ether formation

Doi:10.1039/d1cy00186h
(2021)
Doi:10.1016/0040-4039(78)80034-3
(1978)
One-pot synthesis and radical scavenging activity of novel polyhydroxylated 3-arylcoumarins

Doi:10.1016/j.ejmech.2014.03.053
(2014)
Doi:10.1021/jo01318a018
(1979)
Doi:10.1021/ja00483a042
(1978)

Article Doi