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ChemInform Abstract: ORIGIN OF THE RATE ACCELERATION IN THE IRELAND-CLAISEN REARRANGEMENT. Claisen-rearrangement-mediated ring contraction of macrocyclic lactones. A chemical consequence of the vinylogous anomeric effect. Selective mono-claisen rearrangement of carbohydrate glycals. Nachrichten aus Chemie, Technik und Laboratorium 1988, 520-522. Correlation methods for analyzing and predicting reactivities in nucleophilic substitution processes. European Journal of Organic Chemistry 1998, 1998

The Effects of Substituents on the Degenerate Cope Rearrangement of Semibullvalenes and Barbaralanes. Jackman, Errol Fernandes, Markus Heubes, Helmut Quast. indacene ring system of (-)-spinosyn A via transannular Diels-Alder reactions of substituted ( Studies on the synthesis of the decahydro.

Scott A Frank, Andrea B Works, William R Roush.

Claisen Rearrangements in Carbohydrate Chemistry. The Ireland–Claisen rearrangement as a probe for the diastereoselectivity of nucleophilic attack on a double bond adjacent to a stereogenic centre carrying a silyl group. Adam Levine Debuts Must-See Rose Face Tattoo. Diastereoselective Claisen Rearrangements. John Travolta Praises 'Amazing' Daughter Ellas Singing Skills. Highly regioselective decarboxylative Claisen rearrangement reactions of diallyl 2-sulfonylmalonates. A quantitative structure–reactivity relationship in decarboxylative Claisen rearrangement reactions of allylic tosylmalonate esters. Syntheses and Uses of Isotopically Labelled Dienes and Polyenes.

MieczysÅaw ZieliÅski, Marianna KaÅska.

Investigation of quantitative structure–reactivity relationships in the aliphatic Claisen rearrangement of bis-vinyl ethers reveals a dipolar, dissociative mechanism. 6.16 Functional Group Transformation via Allyl Rearrangement. Mechanisms and Dynamics of Reactions Involving Entropic Intermediates.

Jamieson, Xiao-Song Xue, Marc Garcia-Borràs, Tyler Benton, Xiaofei Dong, Fang Liu, K.N. The Journal of Organic Chemistry 1996, 61 Sequential 1,4-Addition and Ireland−Claisen Rearrangement Promoted by a Manganese−PbCl2−Me3SiCl System1.

Kazuhiko Takai, Takashi Ueda, Hiroya Kaihara, Yoichi Sunami, and, Toshio Moriwake.

Journal of the American Chemical Society 1997, 119 Theory of Substituent Effects on Pericyclic Reaction Rates: Alkoxy Substituents in the Claisen Rearrangement.

Response to Solvents and Substituents: The Case for Both Hydrophobic and Hydrogen Bond Acceleration in Water and for a Variable Transition State. The Journal of Organic Chemistry 1997, 62 Analysis of Substituent Effects on the Claisen Rearrangement with Ab Initio and Density Functional Theory. Viktorya Aviyente,, Hi Young Yoo and, K.Claisen Rearrangement over the Past Nine Decades. The Journal of Organic Chemistry 2015, 80 Base-Mediated Cascade Rearrangements of Aryl-Substituted Diallyl Ethers. This article is cited by 26 publications.