Diastereoselective Addition of Diazomethane to Zaluzanin A
نویسندگان
چکیده
منابع مشابه
1,4- Addition of diazomethane to a heterodiene: a direct preparation of the oxazolic ring.
The reaction of naphthoquinone-oximes (3) and (4) with diazomethane yields directly, in one step, the oxazoles (5) and (6), respectively.
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In this report, we have presented the first diastereoselective addition of phenylacetylene to chiral racemic chloroketones. The addition is controlled by the reactivity of the chloroketones that allowed the stereoselective reaction to be performed at -20 °C. Chiral racemic chloroketones are used in the reaction. By carefully controlling the temperature and the reaction time we were able to isol...
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The current realm of Lewis acid-promoted propargylsilane additions to carbonyl groups2 may be subdivided into two mechanistically distinct categories: (i) additions proceeding via a desilylation pathway;3 (ii) additions involving a [1,2]-silyl shift.4 Process (i) generates allenic alcohols and is most common when nonbulky silyl groups such as TMS are employed,3 whereas the latter scenario has b...
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[reaction: see text] Treatment of hydroxy-substituted silyl epoxides with Grignard reagents induces a 1,2-carbon shift to reveal alpha-silyl aldehydes, which are trapped by highly diastereoselective addition reactions of the Grignard reagent. The starting epoxides are readily accessible from propargylic alcohols by regio- and diastereoselective hydrosilylation and epoxidation reactions. In addi...
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chapter i provides an overview of structural linguistics and touches upon the saussurean dichotomies with the final goal of exploring their relevance to the stylistic studies of literature. to provide evidence for the singificance of the study, chapter ii deals with the controversial issue of linguistics and literature, and presents opposing views which, at the same time, have been central to t...
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ژورنال
عنوان ژورنال: Natural Product Communications
سال: 2014
ISSN: 1934-578X,1555-9475
DOI: 10.1177/1934578x1400900605