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Volumn 73, Issue 13, 2008, Pages 5119-5122

Aryl-aryl bond formation by flash vacuum pyrolysis of benzannulated thiopyrans

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; CHEMICAL REACTIONS; HYDROCARBONS; KETONES; ORGANIC COMPOUNDS; PYROLYSIS; SULFUR; SULFUR COMPOUNDS; THERMOGRAVIMETRIC ANALYSIS; THIOPHENE; VACUUM;

EID: 46849088195     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800379x     Document Type: Article
Times cited : (4)

References (48)
  • 1
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    • For many examples, see
    • For many examples, see: Tsefrikas, V. M.; Scott, L. T Chem. Rev. 2006, 106, 4868-4884.
    • (2006) Chem. Rev , vol.106 , pp. 4868-4884
    • Tsefrikas, V.M.1    Scott, L.T.2
  • 3
    • 46849095499 scopus 로고    scopus 로고
    • Hill, T. J.; Hughes, R. K.; Scott, L. T. Abstracts of Papers, 234th ACS National Meeting; Boston, MA, August 19-23, 2007; abstr. no. ORGN-748.
    • (a) Hill, T. J.; Hughes, R. K.; Scott, L. T. Abstracts of Papers, 234th ACS National Meeting; Boston, MA, August 19-23, 2007; abstr. no. ORGN-748.
  • 4
    • 46849111869 scopus 로고    scopus 로고
    • Hill, T. J. Ph.D. Dissertation, Boston College, 2007.
    • (b) Hill, T. J. Ph.D. Dissertation, Boston College, 2007.
  • 7
    • 46849120470 scopus 로고    scopus 로고
    • Tsefrikas, V. M. Ph.D. Dissertation,Boston College, 2007.
    • (b) Tsefrikas, V. M. Ph.D. Dissertation,Boston College, 2007.
  • 10
    • 85055157760 scopus 로고    scopus 로고
    • A value of 78.3 kcal/mol for the C-S bond dissociation energy of Ph-S-Ph is reported by: (a) Luo, Y.-R. Handbook of Bond Dissociation Energies in Organic Compounds; CRC Press: Boca Raton, FL, 2002. Using the Benson additivity tables, a value of 76 kcal/mol has been estimated for the BDE of Ph-S-Ph by.
    • A value of 78.3 kcal/mol for the C-S bond dissociation energy of Ph-S-Ph is reported by: (a) Luo, Y.-R. Handbook of Bond Dissociation Energies in Organic Compounds; CRC Press: Boca Raton, FL, 2002. Using the Benson additivity tables, a value of 76 kcal/mol has been estimated for the BDE of Ph-S-Ph by.
  • 12
    • 46849086231 scopus 로고    scopus 로고
    • 7e together with calculated heats of formation of Ph-S-Ph, fall in the range of 77.7 to 81.6 kcal/mol (PM3 and AM1 levels of theory, respectively).
    • 7e together with calculated heats of formation of Ph-S-Ph, fall in the range of 77.7 to 81.6 kcal/mol (PM3 and AM1 levels of theory, respectively).
  • 29
    • 0033880102 scopus 로고    scopus 로고
    • Details of the technique and the apparatus used are described in ref 1 and in: Necula, A.; Scott, L. T. J. Anal. Appl. Pyrolysis 2000, 54, 65-87.
    • Details of the technique and the apparatus used are described in ref 1 and in: Necula, A.; Scott, L. T. J. Anal. Appl. Pyrolysis 2000, 54, 65-87.
  • 30
    • 37549055145 scopus 로고    scopus 로고
    • Benzo[kl]thioxanthene (1) was prepared according to the procedure of: De Luca, G.; Pizzabiocca, A.; Renzi, G Tetrahedron Lett. 1983, 24, 821-824.
    • Benzo[kl]thioxanthene (1) was prepared according to the procedure of: De Luca, G.; Pizzabiocca, A.; Renzi, G Tetrahedron Lett. 1983, 24, 821-824.
  • 31
    • 46849118851 scopus 로고    scopus 로고
    • 1H NMR spectra of the pyrolysis mixtures prior to any separation of the components.
    • 1H NMR spectra of the pyrolysis mixtures prior to any separation of the components.
  • 33
    • 84985216572 scopus 로고    scopus 로고
    • Benzo[b]naphtho[1,2-d]thiophene (3) was prepared according to the procedure of: Tominaga, Y.; Lee, M. L.; Castle, R. N. J. Heterocycl. Chem. 1981, 18, 967-972.
    • Benzo[b]naphtho[1,2-d]thiophene (3) was prepared according to the procedure of: Tominaga, Y.; Lee, M. L.; Castle, R. N. J. Heterocycl. Chem. 1981, 18, 967-972.
  • 35
    • 85034475798 scopus 로고
    • and references cited therein
    • Brown, R. F. C.; Eastwood, F. W. Synlett 1993, 9-19, and references cited therein.
    • (1993) Synlett , pp. 9-19
    • Brown, R.F.C.1    Eastwood, F.W.2
  • 36
    • 1642333104 scopus 로고    scopus 로고
    • Naphtho[2,1,8,7-klmn]thioxanthene (6) was prepared according to the procedure of: Donovan, P. M.; Scott, L. T. J. Am. Chem. Soc. 2004, 126, 3108-3112.
    • Naphtho[2,1,8,7-klmn]thioxanthene (6) was prepared according to the procedure of: Donovan, P. M.; Scott, L. T. J. Am. Chem. Soc. 2004, 126, 3108-3112.
  • 37
    • 46849121666 scopus 로고    scopus 로고
    • Necula, A. Ph.D. Dissertation, Boston College, 1996.
    • (a) Necula, A. Ph.D. Dissertation, Boston College, 1996.
  • 38
    • 37049085144 scopus 로고    scopus 로고
    • Sarobe, M.; Zwikker, J. W.; Snoeijer, J. D.; Wiersum, U. E.; Jenneskens, L. W. J. Chem. Soc., Chem. Commun. 1994, 89-90, Erratum: J. Chem. Soc., Chem. Commun. 1994, 1404.
    • (b) Sarobe, M.; Zwikker, J. W.; Snoeijer, J. D.; Wiersum, U. E.; Jenneskens, L. W. J. Chem. Soc., Chem. Commun. 1994, 89-90, Erratum: J. Chem. Soc., Chem. Commun. 1994, 1404.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.