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  • 1
    ISSN: 1434-193X
    Keywords: Amino acids ; Bicyclopropylidene ; Methylenespiropentane ; Spiro compounds ; Organolithium derivatives ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Racemic bicyclopropylidenyl- (rac-11) and methylenespiropentyl- (rac-17) substituted alanines have been synthesized by iodination of bicyclopropylidenyl- and methylenespiropentylmethanols 7, 13, nucleophilic substitution of the iodine in 8, 14 with the enolate of ethyl α-(diphenylmethyleneamino)acetate (O'Donnell's glycine equivalent) and deprotection of 9, 15 in 24 and 18% overall yield, respectively. N-Methylbicyclopropylidenylalanine rac-22, was obtained from the Michael adduct of (bicyclopropylidenyl)magnesium bromide 18 to enamine 19 and deprotection of the carbamate 20 (23% overall yield). Racemic (1-amino-2-methylenespiropentane)- (37), (1-amino-2-methylenecyclopropane)- (3), and (1-aminobicyclopropylidene)carboxylic acid (39) were prepared as hydrochlorides by tert-butoxycarbonylation of the lithiated methylenespiropentane (6), methylenecyclopropane (4), or bicyclopropylidene (5) intermediates with di-tert-butyl pyrocarbonate (Boc2O), repeated lithiation of the tert-butyl esters 29, 30, and 33 with LDA and subsequent carboxylation, Curtius degradation of the half esters 31, 32, and 34 followed by deprotection in 11, 45, and 4% overall yields, respectively. Compound 37 was also prepared from bicyclopropylidene (5) following the same procedure, but with rearrangement in the last but one step, in 19% overall yield. An attempted Hofmann degradation of the bicyclopropylidenecarboxamido ester 40 with NBS failed and gave only bromohydrin 44 (27%), but with bis(acetoxy)iodobenzene provided carbamate 46a, b in 76 amd 79% yield, respectively. Along this route with subsequent deprotection of 46b, the amino acid 39 could be prepared in up to 10% overall yield from bicyclopropylidene.
    Additional Material: 1 Ill.
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  • 2
    ISSN: 1434-193X
    Keywords: Bicyclopropylidene ; [3 + 2] Co-cyclization ; Nickel(0) catalysis ; Palladium(0) catalysis ; 4-Methylenespiro[2.4]heptane derivatives ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bicyclopropylidene (1) readily undergoes a palladium(0)-catalyzed [3 + 2] co-cyclization with electron deficient alkenes (methyl acrylate, methyl trans-crotonate, methyl cinnamate and diethyl fumarate) as well as with some strained alkenes (norbornene, norbornadiene) by distal ring cleavage of one of the three-membered rings of 1. All these co-cyclizations are regioselective with respect to 1 as well as regio- and stereoselective with respect to the alkenes to give the corresponding 4-methylenespiro[2.4]heptane-trans-6-carboxylates 2a-5 with the electron deficient alkenes and the cycloadducts 6 and 7 with the strained alkenes in acceptable to good yields (56 to 83%). In contrast to palladium(0) catalysts nickel(0) complexes catalyze both distal ring opening of 1 and oxidative coupling of the two double bonds when 1 is reacted with e.g. diethyl fumarate. The result is a mixture of the methylenecyclopentane derivative 5 with the [2 + 2] cycloadduct 8 and the cotrimer 9.
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  • 3
    ISSN: 1434-193X
    Keywords: Amino acids ; Bicyclopropylidene ; Methylenecyclopropane ; Palladium catalysis ; Zinc reagents ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Palladium-catalyzed cross-coupling reactions of bromo(methylenecyclopropanes) 1c, 2c with the sodium enolate of dimethyl malonate 4a and the chlorozinc enolates of the glycine equivalent (diphenylmethyleneamino)acetate 4c and diethyl malonate 4d, respectively, have been found to proceed with opening of the three-membered ring in each case, to give the corresponding dienyl-substituted CH-acidic compounds 5-7 in moderate to good yields. On the other hand, coupling of bicyclopropylidenylzinc chloride (2d) with diethyl bromomalonate (4e) and the electrophilic glycine equivalent ethyl 2-acetoxy-2-(diphenylmethyleneamino)acetate (4f) gave 7 and 6 in 27 and 29% yield, respectively.
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  • 4
    ISSN: 0947-3440
    Keywords: Bicyclopropylidene ; Spiro compounds ; Cycloadditions ; Amino acids ; Cuprates ; Tetrahydropyridines ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of ethyl 2-acetoxy-2-diphenylmethyleneaminoacetate (1) with organocopper reagents derived from bicyclopropylidene (2) and methylenecyclopropane (3) are accompanied by an unusual mode of opening of one three-membered ring to give 4-methylene-1,2,3,4-tetrahydropyridine derivatives 8a, 9 in good yields. The cuprate derived from methylenespiropentane (4) reacts with 1 to yield both the normal substitution product 14 (37%) as well as the rearrangement product 15 (34%), while the simple cyclopropylcuprate undergoes substitution to give the protected cyclopropylglycine 16 (75%) without rearrangement. The tetrahydropyridine 8a shows an interesting tautomerism in solution. The 4-cyclopropylidenetetrahydropyridine 15 undergoes an unusual dehydrodimerization to produce two separable rotamers, C2-19 and C1-19, via 18.
    Additional Material: 3 Ill.
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