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Pregled bibliografske jedinice broj: 81567

Sulfur-bridged molecular racks: O, S- sesquinorbornadienes, CNS-[3] and CNOS- [4]polynorbornanes


Margetić, Davor; Butler, Douglas N.; Warrener, R. N.
Sulfur-bridged molecular racks: O, S- sesquinorbornadienes, CNS-[3] and CNOS- [4]polynorbornanes // ARKIVOC, (2002), 6; 234-256 doi:10.3998/ark.5550190.0003.621 (međunarodna recenzija, članak, znanstveni)


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Naslov
Sulfur-bridged molecular racks: O, S- sesquinorbornadienes, CNS-[3] and CNOS- [4]polynorbornanes

Autori
Margetić, Davor ; Butler, Douglas N. ; Warrener, R. N.

Izvornik
ARKIVOC (1551-7004) (2002), 6; 234-256

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
thianorbornenes ; cycloaddition ; AM1 ; modelling ; high-pressure

Sažetak
Thiophene has been reacted under high-pressure (10 kbar) and temperature (100(0)C) with N- methylmaleimide and N-phenylmaleimide to produce Diels-Alder exo- and endo-adducts in modest yields (25-36%). Reaction of 7-oxanorbornadiene-2, 3- dicarboxylic anhydride 6, a highly reactive dienophile, with thiophene occurred under high- pressure (10 kbar) at 100degreesC to yield stereoisomeric 1:1-adducts by site selective attack at the maleic anhydride type of p-bond. This approach afforded the first examples of syn- and anti- heterobridged sesquinorbornadiene anhydrides 8 and 9 containing a sulfur bridge. Similar reaction of isobenzothiophene with 6 was even more facile as reaction occurred at room temperature and atmospheric pressure to yield benzo-analogues 12 and 13. Thermal fragmentation involving loss of furan and sulfur occurred from both classes of adducts under FVP (370 C-0, 0.005 mbar) to produce phthalic anhydride or naphthalene-2, 3-dicarboxylic anhydride respectively. The putative 7-thianorbornadiene intermediates 20 and 22, generated by loss of furan, were not detected. Reaction of exo-N-methyl 7-thianorbornene-5, 6- dicarboxylic imide 4a with the ester-activated cyclobutenoaziridine 16 provided access to CNS- [3]polynorbornane 18, while similar addition of the exo, endo-isomer of O, S-benzosesquinorbornadiene 13 to 16 afforded the CNOS-[4]polynorbornane 19. These are the first S-bridged [n]polynorbornanes to be reported. Molecular modelling (AM1) has shown that S- n-[n]polynorbornadienes have a curved topology greater than O-n-[n]polynorbornadienes but less than N-n-[n]polynorbornadienes.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Profili:

Avatar Url Davor Margetić (autor)

Poveznice na cjeloviti tekst rada:

doi quod.lib.umich.edu

Citiraj ovu publikaciju:

Margetić, Davor; Butler, Douglas N.; Warrener, R. N.
Sulfur-bridged molecular racks: O, S- sesquinorbornadienes, CNS-[3] and CNOS- [4]polynorbornanes // ARKIVOC, (2002), 6; 234-256 doi:10.3998/ark.5550190.0003.621 (međunarodna recenzija, članak, znanstveni)
Margetić, D., Butler, D. & Warrener, R. (2002) Sulfur-bridged molecular racks: O, S- sesquinorbornadienes, CNS-[3] and CNOS- [4]polynorbornanes. ARKIVOC, (6), 234-256 doi:10.3998/ark.5550190.0003.621.
@article{article, author = {Margeti\'{c}, Davor and Butler, Douglas N. and Warrener, R. N.}, year = {2002}, pages = {234-256}, DOI = {10.3998/ark.5550190.0003.621}, keywords = {thianorbornenes, cycloaddition, AM1, modelling, high-pressure}, journal = {ARKIVOC}, doi = {10.3998/ark.5550190.0003.621}, number = {6}, issn = {1551-7004}, title = {Sulfur-bridged molecular racks: O, S- sesquinorbornadienes, CNS-[3] and CNOS- [4]polynorbornanes}, keyword = {thianorbornenes, cycloaddition, AM1, modelling, high-pressure} }
@article{article, author = {Margeti\'{c}, Davor and Butler, Douglas N. and Warrener, R. N.}, year = {2002}, pages = {234-256}, DOI = {10.3998/ark.5550190.0003.621}, keywords = {thianorbornenes, cycloaddition, AM1, modelling, high-pressure}, journal = {ARKIVOC}, doi = {10.3998/ark.5550190.0003.621}, number = {6}, issn = {1551-7004}, title = {Sulfur-bridged molecular racks: O, S- sesquinorbornadienes, CNS-[3] and CNOS- [4]polynorbornanes}, keyword = {thianorbornenes, cycloaddition, AM1, modelling, high-pressure} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


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