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ChemInform Abstract: Selective Reduction of the Carbonyl Group in Organomercurials. A Facile Method for the Protection-Deprotection of the Mercurio Group and a New Route to Annulated Lactones.

✍ Scribed by P. KOCOVSKY; V. DUNN; J. M. GRECH; J. SROGL; W. L. MITCHELL

Book ID: 112039493
Publisher: John Wiley and Sons
Year: 2010
Weight: 31 KB
Volume: 27
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199644115

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Selective reduction of the carbonyl grou

Selective reduction of the carbonyl group in organomercurials. A facile method for the protection-deprotection of the mercurio group and a new route to annulated lactones

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ChemInform Abstract: An Approach Toward the Triquinane-Type Skeleton via Reagent-Controlled Skeletal Rearrangements. A Facile Method for Protection—Deprotection of Organomercurials, Tuning the Selectivity of Wagner—Meerwein Migrations, and a New Route to Annulated Lactones.

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## 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 v

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ChemInform Abstract: Selective Deprotect

ChemInform Abstract: Selective Deprotection of the Cbz Amine Protecting Group for the Facile Synthesis of Kanamycin A Dimers Linked at N-3′′ Position.

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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 v

A novel method for protection and deprot

A novel method for protection and deprotection of the carbonyl groups in 1,2-indanedione by conversion to dioxa-dithiapropellanes

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1,2-Indanedione reacts with two equivalents of 2-mercaptoethanol to produce, instead of the expected 1,2-bis(1,3oxathiolane), a dioxa-dithia[4.4.3] propellane. Other 1,2-indanediones produce analogous compounds. The protecting groups are removed at room temperature with NBS in aqueous acetone, to pr

A Novel Method for Protection and Deprot

A Novel Method for Protection and Deprotection of the Carbonyl Groups in 1,2-Indanedione by Conversion to Dioxa-Dithiapropellanes.

✍ Joseph Almog; Yirmi Zehavy; Shmuel Cohen 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 82 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.