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Aza Cope Rearrangement

The aza-Cope rearrangement is a concerted process, and it usually takes place via a chairlike transition state where the substituents are arranged in a quasi-equatorial position. (See more detail in Cope rearrangement.) [Pg.22]

The tandem cationic aza-Cope rearrangement followed by a Mannich cyclization was applied in the synthesis of the novel tricyclic core structure of the powerful immunosupressant FR901483 in the laboratory of K. Brummond. Their approach was the first synthetic example in which this tandem reaction passes through a bridgehead iminium ion. [Pg.22]

Bennett et al. developed a facile synthesis of A/-benzylallylglycine based on a tandem 2-aza-Cope/iminium ion solvolysis reaction. ° A/-Benzylallylglycine can be prepared in good yield through a one-pot reaction of N-benzylhomoallylamine with glyoxylic acid monohydrate in methanol. [Pg.23]

During the enantioselective total syntheses of (-)- and (+)-strychnine and the Wieland-Gumlich aldehyde, L.E. Overman and co-workers used the tandem aza-Cope rearrangement/Mannich reaction as a key step. This central aza-Cope/Mannich reorganization step proceeded in 98% yield. [Pg.23]


TL2733,82TL2737). The reaction proceeds through an aza-Cope rearrangement of the initially formed iminium salt, followed by intramolecular cyclization. [Pg.122]

Cartion-cartxin bond formation via tandem Mannich condensation, cationic aza-Cope rearrangement of homoaHylarrunes, leading to pyrolidmes... [Pg.283]

Migration from nitrogen to carbon is observed also in aza-Cope rearrangement [76] Ring expansion occurs in thermal rearrangement of azindine denvauves [77] (equation 17)... [Pg.918]

The aza-Cope/Mannich reaction takes advantage of the facility with which a y,<5-unsaturated itninium ion, such as 6, participates in a [3,3] sigmatropic rearrangement to give an isomeric species which is suitably functionalized for an intramolecular and irreversible Mannich cyclization (see intermediate 7). The aza-Cope rearrangement substrate 6 is simply an unsaturated iminium ion which can be fashioned in a number of ways from a homoallylic... [Pg.642]

With certain substituents, such as methoxy150 or (substituted) phenyl53 functions, in the allylie position the reaction outcome completely changes, giving rise to predominant or exclusive formation of five-membered ring products via a preceding 2-aza-Cope rearrangement of the initially formed A -acyliminium ion. These substituents clearly stabilize the intermediary carbo-cation 3. [Pg.845]

By Tertiary Allylic Amines Zwitterionic Aza-Cope Rearrangement. . . 190... [Pg.157]

Abstract The photoinduced reactions of metal carbene complexes, particularly Group 6 Fischer carbenes, are comprehensively presented in this chapter with a complete listing of published examples. A majority of these processes involve CO insertion to produce species that have ketene-like reactivity. Cyclo addition reactions presented include reaction with imines to form /1-lactams, with alkenes to form cyclobutanones, with aldehydes to form /1-lactones, and with azoarenes to form diazetidinones. Photoinduced benzannulation processes are included. Reactions involving nucleophilic attack to form esters, amino acids, peptides, allenes, acylated arenes, and aza-Cope rearrangement products are detailed. A number of photoinduced reactions of carbenes do not involve CO insertion. These include reactions with sulfur ylides and sulfilimines, cyclopropanation, 1,3-dipolar cycloadditions, and acyl migrations. [Pg.157]

Pd2(dba)3/l,4-bis(diphenylphosphino)butane (DPPB) in the presence of 2-mercaptobenzoic acid <95TL1267>. The Af-allylindolines can be easily oxidized to the corresponding indoles at room temperature with o-chloranil. Additionally, Al-allylanilines were also found to undergo aromatic 3-aza-Cope rearrangements in the presence of Zeolite catalysts to give indoline derivatives as the major product <96TL5281>. [Pg.106]

As expected, some sequences also occur where a domino anionic/pericyclic process is followed by another bond-forming reaction. An example of this is an anionic/per-icyclic/anionic sequence such as the domino iminium ion formation/aza-Cope/ imino aldol (Mannich) process, which has often been used in organic synthesis, especially to construct the pyrrolidine framework. The group of Brummond [450] has recently used this approach to synthesize the core structure 2-885 of the immunosuppressant FR 901483 (2-886) [451] (Scheme 2.197). The process is most likely initiated by the acid-catalyzed formation of the iminium ion 2-882. There follows an aza-Cope rearrangement to produce 2-883, which cyclizes under formation of the aldehyde 2-884. As this compound is rather unstable, it was transformed into the stable acetal 2-885. The proposed intermediate 2-880 is quite unusual as it does not obey Bredf s rule. Recently, this approach was used successfully for a formal total synthesis of FR 901483 2-886 [452]. [Pg.185]

The second largest group of pericyclic domino reactions starts with a sigmatropic rearrangement, which is most often a Claisen or an oxa- and aza-Cope rearrangement however, some processes also exist with a 2,3-sigmatropic rearrangement as the second step. [Pg.280]

A domino Claisen/ene strategy was employed for the synthesis of (+)-9(l l)-dehy-droestrone [82] methyl ether, while an example of a domino aza-Cope rearrange-ment/Mannich reaction is the above-mentioned synthesis of (-)-preussin (4-14) [5]. [Pg.313]

Rearrangement of allylic acetals. 3-Acetylpyrrolidines can be obtained in good yield by an acid-catalyzed rearrangement of 5-methyl-5-vinyloxazolidines. The rearrangement involves an aza-Cope rearrangement followed by Mannich cycli-zation (equation I).1... [Pg.304]

Quaternary allenylallylammonium salts, produced in situ by prototropic isomerization of propargyl precursors (see Section 7.2.2), can undergo a 3-aza-Cope rearrangement [370]. The resulting intermediates are hydrolyzed under the reaction conditions to yield 2 -methylenepent-4-enals. [Pg.413]

In addition to a-allenic a-amino acids, the corresponding allenic derivatives of y-aminobutyric acid (GABA) have also been synthesized as potential inhibitors of the pyridoxal phosphate-dependent enzyme GABA-aminotransferase (Scheme 18.49) [131,138-142]. The synthesis of y-allenyl-GABA (152) and its methylated derivatives was accomplished through Crabbe reaction [131], aza-Cope rearrangement [138] and lactam allenylation [139], whereas the fluoroallene 153 was prepared by SN2 -reduc-tion of a propargylic chloride [141]. [Pg.1027]

TV-Glycosyl homoallylamines have been shown to undergo a stereocontrolled Lewis acid-catalyzed aza-Cope rearrangement to produce chain-extended amino sugars85. The reactions proceed in good to excellent yields with high stereoselectivity. Schiff base... [Pg.726]

The mechanism involves conversion of V-homoallylamine 116a to imine 117a via a Lewis acid-catalyzed cationic aza-Cope rearrangement (equation 61). Various Lewis acids were tested with yields ranging from 40-99% with high diastereoselectivities. [Pg.727]

Fivefold degenerate reversible [3,3]-sigmatropic shifts were first reported in 1988116,117 in the CPD-amidine system 257, where AG g = 117 to 120 kJmol-1 (equation 88) (for aza-Cope rearrangements see Section IV.E.2). In addition, a slow accumulation of a colored by-product was observed at elevated temperatures. This was identified as a product of a novel intramolecular carbon to nitrogen 1,4-shift of the methoxycarbonyl... [Pg.783]

There is no unity of opinion in the literature concerning a classification, i.e, whether to call these transformations aza-Claisen or aza-Cope rearrangements. It is accepted that the term aza-Claisen should be reserved only for those processes in which a carbon atom in the allyl vinyl ether system has been replaced by nitrogen357. Three different types of aliphatic 3-aza-Cope reactions which were studied theoretically are the rearrangements of 3-aza-l,5-hexadienes (610, equation 262), 3-azonia-l,5-hexadienes (611, equation 263) and 3-aza-l,2,5-hexatrienes (612, equation 264) (the latter is a ketenimine rearrangement )357. [Pg.868]

However, a better known version of the 2-aza-Cope rearrangement is that carried out by using 2-aza-l,5-hexadienes 619 (equation 269) and particularly their iminium ion counterparts, usually N-acyliminium cations 620 (equation 270)365,366 (for reviews, see also Reference 367). Aza-Cope rearrangement of the norbomene ester 621 leads to tetrahydropyridine ester 622 when allowed to stand in solution at room temperature for... [Pg.870]

There are few examples of 1-aza-Cope rearrangements, e.g. the transformation of a-hydroxyimines 623 to aminoketones 624 in refluxing diglyme (equation 273)374. Diels-... [Pg.872]


See other pages where Aza Cope Rearrangement is mentioned: [Pg.63]    [Pg.641]    [Pg.642]    [Pg.643]    [Pg.643]    [Pg.652]    [Pg.789]    [Pg.797]    [Pg.1445]    [Pg.1452]    [Pg.174]    [Pg.152]    [Pg.190]    [Pg.24]    [Pg.318]    [Pg.250]    [Pg.55]    [Pg.73]    [Pg.740]    [Pg.868]    [Pg.870]    [Pg.872]    [Pg.149]   
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3-Aza-4-oxa-Cope rearrangements

Aza-Cope

Aza-Cope rearrangement-Mannich cyclization reaction

Aza-Cope rearrangement/Mannich

Aza-Cope rearrangement/Mannich cyclization

Aza-Cope rearrangment

Cationic aza-Cope rearrangement

The Amino- and Aza-Cope Rearrangements

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