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2.
Richard A. Bunce James E. Schammerhorn Jessica Sigle 《Journal of heterocyclic chemistry》2013,50(2):373-380
A tandem imine addition‐SNAr annulation reaction has been developed as a new approach to the synthesis of 4‐oxo‐1,2,3,4‐tetrahydroquinoline‐3‐carboxylic esters. A series of these structures has been generated by reacting selected imines with tert‐butyl 2‐fluoro‐5‐nitrobenzoylacetate. Structural variations in the final products are accomplished by changing the substituents on the imine and the alkyl group of the ester. The title compounds are isolated as their enols in 55–97% yield without the need for added base or catalysts. The synthesis of the starting materials as well as mechanistic studies and further synthetic conversions of the products are presented. 相似文献
3.
G. R. Bunce 《Journal of Optimization Theory and Applications》1977,22(4):563-606
A maximum principle is obtained for control problems involving a constant time lag τ in both the control and state variables. The problem considered is that of minimizing $$I(x) = \int_{t^0 }^{t^1 } {L (t,x(t), x(t - \tau ), u(t), u(t - \tau )) dt} $$ subject to the constraints 1 $$\begin{gathered} \dot x(t) = f(t,x(t),x(t - \tau ),u(t),u(t - \tau )), \hfill \\ x(t) = \phi (t), u(t) = \eta (t), t^0 - \tau \leqslant t \leqslant t^0 , \hfill \\ \end{gathered} $$ 1 $$\psi _\alpha (t,x(t),x(t - \tau )) \leqslant 0,\alpha = 1, \ldots ,m,$$ 1 $$x^i (t^1 ) = X^i ,i = 1, \ldots ,n$$ . The results are obtained using the method of Hestenes. 相似文献
4.
A problem of Mackey for von Neumann algebras has been settled by the conjunction of the early work of Gleason and the recent advances of Christensen and Yeadon. We show that Mackey's conjecture holds in much greater generality. LetA be a JBW-algebra and letL be the lattice of all projections inA. A quantum measure onL is a countably additive map,m, fromL into the real numbers. Our results imply thatm always has a unique extension to a bounded linear functional onA, provided thatA has no TypeI
2 direct summand. 相似文献
5.
Richard A. Bunce David Rogers Takahiro Nago Scott A. Bryant 《Journal of heterocyclic chemistry》2008,45(2):547-550
Treatment of 2‐fluoro‐5‐nitrobenzyl bromide with active methylene compounds in the presence of excess potassium carbonate in acetone leads to the formation of highly functionalized 4H‐1‐benzopyrans by a tandem SN2‐SNAr reaction sequence. The reaction works well with β‐keto esters, β‐keto sulfones, β‐keto phosphine oxides, β‐keto phosphonates and β‐keto nitriles. The reaction is simple to perform and affords products in 50‐92% yields. 相似文献
6.
Richard A. Bunce Sharadsrikar V. Kotturi Christopher J. Peeples Elizabeth M. Holt 《Journal of heterocyclic chemistry》2002,39(5):1049-1054
A tandem SN2‐Michael addition reaction has been developed for the synthesis of cis‐ and trans‐fused nitrogen and sulfur heterocycles from the cis and trans isomers of ethyl (±)‐(2E)‐3‐[2‐(iodomethyl)cyclo‐hexyl]‐2‐propenoate. Octahydro‐1H‐isoindole‐1‐acetic acid and octahydrobenzo[c]thiophene‐1‐acetic acid derivatives have been prepared and their stereochemistries elucidated using NMR and X‐ray crystallo‐graphic methods. Cyclization substrates for both the cis‐ and the trans‐fused rings are readily available in four steps from known compounds. Yields for the cyclization range from 80‐85% and stereochemical selec‐tivities with respect to the side chain vary from 12.5‐16:1 for the cis‐fused structures to 6‐7.5:1 for the trans‐fused structures. Steric interactions in the transition states for ring closure are proposed to rationalize the observed preferences. 相似文献
7.
Richard A. Bunce Lara B. Johnson Elizabeth M. Holt 《Journal of heterocyclic chemistry》2004,41(4):563-568
An efficient, diastereoselective synthesis of substituted and unsubstituted 2,3,4,5‐tetrahydro‐1H‐1‐benzazepine‐5‐carboxylic esters has been developed based on the tandem reduction‐reductive amination reac tion. Catalytic hydrogenation of a series of 2‐(2‐nitrophenyl)‐5‐oxoalkanoic esters initiates a reaction sequence involving (1) reduction of the aromatic nitro group, (2) condensation of the N‐hydroxylamino (or amino) nitrogen with the side chain carbonyl, and (3) reduction of the seven‐membered cyclic imine. Cyclizations that produce 2‐alkyl‐2,3,4,5‐tetrahydro‐1H‐1‐benzazepine‐5‐carboxylic esters are diastereose lective for the product having the C2 alkyl and the C5 ester groups cis. In these reactions, the transannular ester group exerts a strong stereodirecting effect on the reduction of the cyclic imine intermediate, though not as strong as that observed in previous closures of 2‐alkyl‐1,2,3,4‐tetrahydroquinoline‐4‐carboxylic esters. This decrease in diastereoselectivity is attributed to (1) the greater distance between the ester and the imine double bond and (2) the increased conformational mobility of the larger ring, both of which diminish the stereodirecting effect of the ester. Finally, formation of the seven‐membered ring is sufficiently slow that reaction with the side chain ester group competes with heterocycle formation in several of the reactions. 相似文献
8.
A series of N‐substituted 1,4‐dihydro‐4‐oxo‐1,8‐naphthyridine‐3‐carboxylate esters has been prepared in two steps from ethyl 2‐(2‐chloronicotinoyl)acetate. Treatment of the β‐ketoester with N,N‐dimethylformamide dimethyl acetal in N,N‐dimethylformamide (DMF) gave a 95% yield of the 2‐dimethylaminomethylene derivative. Subsequent reaction of this β‐enaminone with primary amines in DMF at 120oC for 24 h then afforded the target compounds in 47–82% yields by a tandem SNAr‐addition‐elimination reaction. Synthetic and procedural details as well as a mechanistic rationale are presented. 相似文献
9.
10.
A diastereoselective synthesis of 1-methyl-2-alkyl- and 2-alkyl-1,2,3,4-tetrahydroquinoline-4-carboxylic esters has been developed from methyl (2-nitrophenyl)acetate (1). The method involves alkylation of 1 with an allylic halide, ozonolysis of the double bond, and catalytic hydrogenation. The final hydrogenation initiates a tandem sequence involving (1) reduction of the aromatic nitro group, (2) condensation of the aniline or hydroxylamine(8) nitrogen with the side chain carbonyl, (3) reduction of the resulting nitrogen intermediate, and (4) reductive amination of the tetrahydroquinoline with formaldehyde produced in the ozonolysis to give a methyl (+/-)-1-methyl-2-alkyl-1,2,3,4-tetrahydroquinoline-4-carboxylate. Removal of the formaldehyde prior to hydrogenation gives the simple (+/-)-2-alkyl derivatives. The products are isolated in high yield as single diastereomers having the C-2 alkyl group cis to the C-4 carboxylic ester. The reaction has been extended to the synthesis of tricyclic structures with similar high diastereoselection. 相似文献