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Rearrangements synthesis

GABRIEL COLMAN Rearrangement Synthesis of isoquinolines by rearrangement ol phthahmides. [Pg.140]

J ULIA-BRUYLANTS Cyclopropyl Carbinol Rearrangement Synthesis ot allyl halides (usually E] by rearrangement ol cyciopropyl carbirKils acid catalyzed)... [Pg.193]

Hodgson, D.M. Galano, J.M. (2005) Enantioselective Access to Isoquinuclidines by Tropen-one Desymmetrization and HomoaHylic Radical Rearrangement Synthesis of (-F)-Ibogamine. Organic Letters, 1, 2221-2224. [Pg.193]

Djerassi, C. Tokes, L. Mass Spectrometry in Stractural and Stereochemical Problems. XCIII. Further Observations on the Importance of Interatomic Distance in the McLafferty Rearrangement. Synthesis and Fragmentation Behavior of Deuterium-Labeled 12-Oxo Steroids. J. Am. Chem. Soc. 1966,88,536-544. [Pg.324]

Carbocation rearrangements synthesis of camphor from a-pinene... [Pg.218]


See other pages where Rearrangements synthesis is mentioned: [Pg.220]    [Pg.221]    [Pg.316]   
See also in sourсe #XX -- [ Pg.759 ]




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2-Azetidinones, 4- synthesis via Pummerer rearrangement

4-Cyclohepten-1 -ones synthesis via Cope rearrangement

Acyl-Claisen rearrangement synthesis

Allocolchicinoid synthesis Schmidt rearrangement

Amdt-Eistert synthesis Wolff rearrangement

Amino acids, enantioselective synthesis rearrangement

Asymmetric synthesis Claisen rearrangement

Azepines, Beckmann rearrangement synthesis

Beckmann rearrangement amide synthesis

Benzene, hydroxy iodooxidative rearrangement a-tosyloxy ketone synthesis

Bicyclo alkanes synthesis via Cope rearrangement

Bicyclo hex-2-enes, 6- Cope rearrangement synthesis

Biomimetic synthesis Wagner-Meerwein rearrangement

Biotin Synthesis Sulfur Preempts a Beckmann Rearrangement

Carbolines, rearrangement synthesis

Claisen rearrangement in -africanol synthesis

Claisen rearrangement in -sinularene synthesis

Claisen rearrangement in lactone synthesis

Claisen rearrangement in synthesis

Claisen rearrangement synthesis

Claisen rearrangement-Wittig synthesis

Cope rearrangement amino alcohol synthesis

Cope rearrangements eight-membered ring synthesis

Cope rearrangements seven-membered ring synthesis

Cycloaddition/rearrangement synthesis

Cyclobutanes, 1,2-divinylCope rearrangement synthesis

Cyclodecanes synthesis via Cope rearrangement

Cycloheptadienes synthesis via Cope rearrangement

Cycloheptanes synthesis via Cope rearrangement

Cyclooctadienes synthesis via Cope rearrangement

Cyclooctanes synthesis via Cope rearrangement

Cyclopropane, 1 -phenylthio-1 - synthesis via silyl-Pummerer rearrangement

Cyclopropane, synthesis via Pummerer rearrangement

Enantioselective synthesis 3,3]-sigmatropic rearrangements

Favorskii rearrangement, natural product synthesis

Fischer indole synthesis 3,3]-sigmatropic rearrangement

Hetero-Claisen rearrangement, synthesis

Hofmann rearrangement amine synthesis

Hydrazines synthesis via oxoniumylide -rearrangement

Industrial synthesis rearrangement

Ireland-Claisen rearrangement in nonactic acid synthesis

Ireland-Claisen rearrangement natural product synthesis

Ketones synthesis via Claisen rearrangement

Lactams Beckmann rearrangement synthesis

Leukotriene D, 5-deoxyprecursor synthesis via sulfoxide-sulfenate rearrangement

Neber rearrangement natural product synthesis

Neber rearrangement synthesis

Nitrene rearrangements synthesis

Nitrones, synthesis rearrangements

Oxidative rearrangements natural product synthesis

Oxy-Cope rearrangements for synthesis

Oxy-cope rearrangement in synthesis of juvabione

P-Lactams synthesis, via Pummerer rearrangement

Peptides synthesis via Claisen rearrangement

Pinacol rearrangement piperidine synthesis

Propargyl-Claisen rearrangement pyrroles synthesis

Propargyl-Claisen rearrangement synthesis

Quaternary centers synthesis via Ireland rearrangement

RING REARRANGEMENT METATHESIS (RRM) A NEW CONCEPT IN PIPERIDINE AND PYRROLIDINE SYNTHESIS

Ramberg-Backlund rearrangement synthesis

Rearrangement branched-chain sugar synthesis

Rearrangement natural products synthesis

Rearrangement reactions, oxazole synthesis

Rearrangement reactions, oxazole synthesis 2-substituted oxazoles

Rearrangements Fisher indole synthesis

Rearrangements alcohol synthesis

Rearrangements in the synthesis

Ring expansion rearrangement syntheses

Ring synthesis Brook rearrangement

Ring synthesis Claisen rearrangement

Ring synthesis Cope rearrangement

Ring synthesis Ireland-Claisen rearrangement

Ring synthesis Pummerer rearrangement

Sigmatropic rearrangements alcohol synthesis

Sigmatropic rearrangements stereoselective synthesis

Sigmatropic rearrangements synthesis

Sommelet-Hauser rearrangement synthesis

Steroids, Beckmann rearrangement synthesis

Strategy XIV Rearrangements in Synthesis

Strategy XVI Pericyclic Rearrangements in Synthesis Special Methods for Five-Membered Rings

Syntheses Substitutions and Rearrangements Involving Neighboring Group Participation of Dihetero-tricyclodecanes

Synthesis Based on Prototropic Rearrangement

Synthesis Beckmann rearrangements

Synthesis of Degradation and Rearrangement Products

Synthesis of Heteroaromatics via Rearrangement Reactions

Synthesis of biaryls via benzidine rearrangement

Synthesis via Claisen rearrangement

Synthesis via Rearrangement Reactions

Synthesis with rearrangement

Vitamin D3, la,25-dihydroxyprecursor synthesis via Johnson rearrangement

Wender synthesis, Cope rearrangement

Wharton rearrangement synthesis

Williamson synthesis 1.2] Wittig rearrangement

Wittig rearrangement alkene synthesis

Wittig rearrangement aziridine synthesis

Wolff rearrangement amide synthesis

Wolff rearrangement synthesis

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