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Journal ArticleDOI

A stereospecific total synthesis of (+/-)-methylenomycin A. A novel antibiotic possessing an alpha-methylene ketone functionality.

Robert M. Scarborough, +1 more
- 12 Oct 1977 - 
- Vol. 99, Iss: 21, pp 7085-7087
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This article is published in Journal of the American Chemical Society.The article was published on 1977-10-12. It has received 30 citations till now. The article focuses on the topics: Methylenomycin a & Ketone.

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Photochemical reactions as key steps in natural product synthesis

TL;DR: The most important photochemical transformations that have been employed in natural product synthesis are presented and selected total syntheses are discussed as examples, with particular attention given to the photochemical key step and its stereoselectivity.
Journal ArticleDOI

Photochemische Reaktionen als Schlüsselschritte in der Naturstoffsynthese

TL;DR: In this article, die wichtigsten Umsetzungen der photochemie vorgestellt, die auf breiter Front Einzug in die Naturstoffsynthese gehalten haben.
Reference EntryDOI

Maleic Anhydride, Maleic Acid, and Fumaric Acid

TL;DR: In this paper, the development of maleic anhydride, maleic acid, and fumaric acid are reviewed over the past 20 years with literature citations when available, including acid chlorides and reaction products formed from acylation, alkylation, amidation, concerted nonpolar reactions of various kinds, decomposition and decarboxylation.
Journal ArticleDOI

Supramolecular Luminescent Lanthanide Dimers for Fluoride Sequestering and Sensing

TL;DR: The X-ray crystal structure of the europium dimer revealed that the architecture of the scaffold is stabilized by synergistic effects of the Eu�FEu bridging motive, π stacking interactions, and a four-component hydrogen-bonding network, which control the assembly of the two [EuL] entities around the fluoride ion.
Journal ArticleDOI

New methodology for the introduction of sulfur into organic molecules

TL;DR: Anhydrous THF solutions of LiS or LiS2 (or chemically equivalent species) are rapidly and quantitatively formed by the reaction of common yellow sulfur with appropriate stoichiometries of commercially available LiEt3BH.
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