Stereospecific method to E and Z terminal fluoro olefins and its application to the synthesis of 2'-deoxy-2'-fluoromethylene nucleosides as potential inhibitors of ribonucleoside diphosphate reductase

DOI: 10.1021/ja00019a061

Source and publish data:

Journal of the American Chemical Society p. 7439 - 7440 (1991)

Update date:2022-09-26

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Authors:

McCarthy

Matthews

Stemerick

Huber Huber

Bey Bey

Lippert Lippert

Snyder Snyder

Sunkara Sunkara

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Article abstract of DOI:10.1021/ja00019a061

Full text of DOI:10.1021/ja00019a061

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Article Doi

Stereospecific method to E and Z terminal fluoro olefins and its application to the synthesis of 2'-deoxy-2'-fluoromethylene nucleosides as potential inhibitors of ribonucleoside diphosphate reductase

DOI: 10.1021/ja00019a061

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja00019a061

Full text of DOI:10.1021/ja00019a061

Products guided by the article

R&D Labs maybe for 135789-97-8

Relevant to this article

Utilizing an Encapsulated Solution of Reagents to Achieve the Four-Component Synthesis of (Benzo)Thiophene Derivatives

SmI2-PROMOTED KETYL RADICAL ADDITION TO O-BENZYL FORMALDOXIME. A NEW AMINOMETHYLATION

Enantioselective total synthesis of the di-O-methyl ethers of (-)-agatharesinol, (+)-hinokiresinol and (-)-sugiresinol, characteristic norlignans of Coniferae

Asymmetric reductive amination of cycloalkanones. XI. Synthesis of optically active 2-substituted cycloheptanamines

Palladium-catalyzed silyl C(sp3)-H bond activation

Highly chemoselective reduction of carbonyl groups in the presence of aldehydes

Palladium-catalyzed silyl C(sp³)-H bond activation