ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Bicyclopropylidene  (1)
  • Dithioles  (1)
  • Wiley-Blackwell  (2)
  • 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.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1434-193X
    Keywords: Dithioles ; Anthracenes ; Lithiation ; Electron donors ; Crystal structures ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The synthesis of new derivatives of 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene has been achieved by two different routes. Deprotonation of 8 using LDA in THF at -78 °C, followed by in situ quenching of the lithiated intermediate 9 with N,N-dimethylformamide, N-methyl isothiocyanate and methyl chloroformate gave aldehyde, thioamide and methyl ester derivatives 10-12, respectively. Sulfur insertion into the lithiated species 9 followed by reaction of the transient thiolate anion with benzoyl chloride gave the thioester derivative 13 which served as a convenient shelf-stable precursor of other mono-functionalised derivatives of 8. Debenzoylation of 13 and trapping of the transient thiolate anion with iodomethane and 6-bromohexan-1-ol yielded 14 and 15, respectively. Reaction of cation salt 17 with the anion of anthrone 18 gave compound 20, the thiolate anion of which reacted with 6-bromohexan-1-ol to afford the alcohol derivative 21. Subsequent reactions gave alcohol derivative 25 of the title system. The unexpected product 29 was obtained from reaction of 28 with triethyl phosphite. The X-ray crystal structures of compounds 12, 14, 28, and 29 are reported. The molecules adopt a saddle-like conformation; the bis(1,3-dithiole)benzoquinone system is U-shaped through an ‘accumulating bend’ comprising the boat conformation of the central (quinonoid) ring, folding of both 1,3-dithiole rings along S···S vectors, and out-of-plane tilting of the exocyclic C=C bonds, all in the same (inward) direction.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...