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Volumn 12, Issue 5, 2010, Pages 924-927

Rhodium carbenoid approach for introduction of 4-substituted (Z)-pent-2-enoates into sterically encumbered pyrroles and indoles

Author keywords

[No Author keywords available]

Indexed keywords

6 (NITROOXY)HEXYL (2Z) 4 (ACETYLOXY) 3 (4 (METHYLSULFONYL)PHENYL) 2 PHENYLBUT 2 ENOATE; 6-(NITROOXY)HEXYL-(2Z)-4-(ACETYLOXY)-3-(4-(METHYLSULFONYL)PHENYL)-2-PHENYLBUT-2-ENOATE; BUTYRIC ACID DERIVATIVE; INDOLE DERIVATIVE; NITRO DERIVATIVE; ORGANOMETALLIC COMPOUND; PYRROLE DERIVATIVE; RHODIUM;

EID: 77749286097     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol9028385     Document Type: Article
Times cited : (63)

References (34)
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    • 2: Bis[rhodium(αα, α',α',-tetramethyl-l,3-benzenedipropionic acid)]. For a leading reference, see: Zalatan, D. N.; Bois, J. D. J. Am. Chem. Soc. 2009, 131, 7558.
    • 2: Bis[rhodium(αα, α',α',-tetramethyl-l,3-benzenedipropionic acid)]. For a leading reference, see: Zalatan, D. N.; Bois, J. D. J. Am. Chem. Soc. 2009, 131, 7558.
  • 26
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    • Vinylogous reactivity of substituted vinylcarbenoids has been observed with silver catalysis and diruthenium catalysis. For examples, see: (a) Yue, Y, Wang, Y, Hu, W. Tetrahedron Lett. 2007, 48, 3975
    • Vinylogous reactivity of substituted vinylcarbenoids has been observed with silver catalysis and diruthenium catalysis. For examples, see: (a) Yue, Y.; Wang, Y.; Hu, W. Tetrahedron Lett. 2007, 48, 3975.
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    • Ref 9
    • (b) Ref 9.
  • 28
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    • The models used to describe the reactions of vinylcarbenoids have assumed that the reaction occurs through a particular carbenoid conformation. For example, the combined C-H activation/Cope rearrangement and a [3, 2] cycloaddition have been proposed to involve a reaction where the vinylcarbenoid is in the s-cis conformation. For details, see: (a) Davies, H. M. L, Jin, Q. J. Am. Chem. Soc. 2004, 126, 10862
    • The models used to describe the reactions of vinylcarbenoids have assumed that the reaction occurs through a particular carbenoid conformation. For example, the combined C-H activation/Cope rearrangement and a [3 + 2] cycloaddition have been proposed to involve a reaction where the vinylcarbenoid is in the s-cis conformation. For details, see: (a) Davies, H. M. L.; Jin, Q. J. Am. Chem. Soc. 2004, 126, 10862.
  • 29
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    • Recently, we proposed that the [3, 2] annulation of indoles by vinylcarbenoids may occur via the s-trans conformation of the vinylcarbenoid. For details, see
    • (b) Davies, H. M. L.; Xiang, B.; Kong, N.; Stafford, D. G. J. Am. Chem. Soc. 2001, 123, 146. Recently, we proposed that the [3 + 2] annulation of indoles by vinylcarbenoids may occur via the s-trans conformation of the vinylcarbenoid. For details, see:
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 146
    • Davies, H.M.L.1    Xiang, B.2    Kong, N.3    Stafford, D.G.4
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    • Chem. Soc, ASAP
    • (c) Lian, Y.; Davies, H. M. L. J. Am. Chem. Soc. 2010, 132, ASAP.
    • (2010) J. Am , pp. 132
    • Lian, Y.1    Davies, H.M.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.