메뉴 건너뛰기




Volumn 29, Issue 11, 2010, Pages 2400-2402

(Selenocarbamoyl)silanes and -germanes: Their synthesis using (selenocarbamoyl)lithium and characterization

Author keywords

[No Author keywords available]

Indexed keywords

GERMANES; GOOD YIELD; SILYLATIONS;

EID: 77953223467     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om100290h     Document Type: Article
Times cited : (11)

References (51)
  • 1
    • 0001600151 scopus 로고    scopus 로고
    • For reviews: Wirth, T., Ed.; Springer-Verlag: Berlin
    • For reviews: Murai, T.; Kato, S. In Topics in Current Chemistry; Wirth, T., Ed.; Springer-Verlag: Berlin, 2000; Vol. 208, p 177.
    • (2000) Topics in Current Chemistry , vol.208 , pp. 177
    • Murai, T.1    Kato, S.2
  • 3
    • 21644454681 scopus 로고    scopus 로고
    • For reviews and recent examples of the generation and reaction of selenoaldehydes and -ketones: Back, T. G., Ed.; Oxford University Press: Oxford, U.K
    • For reviews and recent examples of the generation and reaction of selenoaldehydes and -ketones: Guziec, F. S., Jr.; Guziec, L. J. In Organoselenium Chemistry: A Practical Approach; Back, T. G., Ed.; Oxford University Press: Oxford, U.K., 1999; p 193.
    • (1999) Organoselenium Chemistry: A Practical Approach , pp. 193
    • Guziec Jr., F.S.1    Guziec, L.J.2
  • 14
    • 21644460853 scopus 로고    scopus 로고
    • For reviews: Katritzky, A. R.; Taylor, R. J. K., Eds.; Elsevier: Oxford, U.K
    • For reviews: Moore, A. J. In Comprehensive Organic Functional Group Transformations; Katritzky, A. R.; Taylor, R. J. K., Eds.; Elsevier: Oxford, U.K., 2005; Vol. 5, p 519.
    • (2005) Comprehensive Organic Functional Group Transformations , vol.5 , pp. 519
    • Moore, A.J.1
  • 16
    • 25444453090 scopus 로고    scopus 로고
    • Kato, S., Ed.; Springer-Verlag: Heidelberg, Germany
    • Murai, T. In Topics in Current Chemistry; Kato, S., Ed.; Springer-Verlag: Heidelberg, Germany, 2005; Vol. 251, p 247.
    • (2005) Topics in Current Chemistry , vol.251 , pp. 247
    • Murai, T.1
  • 20
    • 33845632013 scopus 로고    scopus 로고
    • For a review
    • For a review: Wirth, T. Sci. Synth. 2005, 22, 181
    • (2005) Sci. Synth. , vol.22 , pp. 181
    • Wirth, T.1
  • 21
    • 21644437043 scopus 로고    scopus 로고
    • For reviews
    • For reviews: Murai, T. Synlett 2005, 1509
    • (2005) Synlett , pp. 1509
    • Murai, T.1
  • 22
    • 33748860731 scopus 로고    scopus 로고
    • Kato, S., Ed.; Springer-Verlag: Heidelberg, Germany
    • Ishii, A.; Nakayama, J. In Topics in Current Chemistry; Kato, S., Ed.; Springer-Verlag: Heidelberg, Germany, 2005; Vol. 251, p 227.
    • (2005) Topics in Current Chemistry , vol.251 , pp. 227
    • Ishii, A.1    Nakayama, J.2
  • 23
    • 0001066877 scopus 로고
    • In situ generation of selenoacylsilane and its trapping by a diene has been reported
    • In situ generation of selenoacylsilane and its trapping by a diene has been reported: Segi, M.; Koyama, T.; Nakajima, T.; Suga, S.; Murai, S.; Sonoda, N. Tetrahedron Lett. 1989, 30, 2095
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2095
    • Segi, M.1    Koyama, T.2    Nakajima, T.3    Suga, S.4    Murai, S.5    Sonoda, N.6
  • 24
    • 0012975508 scopus 로고    scopus 로고
    • For recent examples, see
    • For recent examples, see: Murai, T.; Aso, H.; Kato, S. Org. Lett. 2002, 4, 1407
    • (2002) Org. Lett. , vol.4 , pp. 1407
    • Murai, T.1    Aso, H.2    Kato, S.3
  • 33
    • 77953218310 scopus 로고    scopus 로고
    • note
    • 23NSeSi: C, 59.98; H, 6.43; N, 3.89. Found: C, 59.79; H, 6.48; N, 3.90.
  • 34
    • 77953225020 scopus 로고    scopus 로고
    • note
    • 23GeNSe: C, 53.38; H, 5.72; N, 3.46. Found: C, 53.62; H, 5.87; N, 3.39.
  • 35
    • 77953206135 scopus 로고    scopus 로고
    • note
    • The computations were done using Gaussian 03. The hybrid density functional B3LYP along with the 6-311+G(d) basis set was used for the structure optimization and energy calculations. Further technical details are provided in the Supporting Information.
  • 36
    • 15044338850 scopus 로고    scopus 로고
    • For recent examples of carbamoylsilanes
    • For recent examples of carbamoylsilanes: Cunico, R. F.; Motta, A. R. Org. Lett. 2005, 7, 771
    • (2005) Org. Lett. , vol.7 , pp. 771
    • Cunico, R.F.1    Motta, A.R.2
  • 45
    • 77953190713 scopus 로고    scopus 로고
    • note
    • 2 (6) in a procedure that is similar to that used to prepare 3 and 4. The C=S carbons of 6 - 8 resonate at δ 189.5, 224.2, and 225.1, respectively (see the Supporting Information).
  • 46
    • 77953198046 scopus 로고    scopus 로고
    • note
    • In contrast to the generation of carbamoyllithiums (18) and thiocarbamoyllithiums, (19) no studies of their selenium isologues have been reported.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.