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ChemInform Abstract: Highly Stereoselective Radical Reduction of α‐Bromo‐α‐fluoro‐β‐hydroxy Esters with Tributyltin Hydride Leading to threo‐αFluoro‐β‐hydroxy Esters.

Kazuhide Mima, Takashi Ishihara, Saki Kuwahata, Tsutomu Konno, Hiroki Yamanaka

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Abstract

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

About this research paper

What this paper is about

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Why it matters

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Key contribution

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Method / approach

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Main findings

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Available abstract

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Key concepts: Tributyltin hydride, Chemistry, Stereoselectivity, Tributyltin, Reduction (mathematics), Hydride, Combinatorial chemistry, Medicinal chemistry

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ChemInform Abstract: Highly Stereoselective Radical Reduction of α‐Bromo‐α‐fluoro‐β‐hydroxy Esters with Tributyltin Hydride Leading to threo‐αFluoro‐β‐hydroxy Esters. — Research Paper | ScholarLens