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Volumn 66, Issue 31, 2010, Pages 5819-5826

Effects of stereochemistry and β-substituents on the rates of vinylic SN2 reaction of hypervalent vinyl(phenyl)-λ3- iodanes with tetrabutylammonium halides

Author keywords

Hypervalent; Inversion; Iodine; SN2 reaction; Vinyliodane

Indexed keywords

[BETA (2 PHENYLETHOXY)VINYL](PHENYL)TETRAFLUOROBORATO) LAMBDA 3 IODANE; CARBON; HALIDE; IODINE; TETRABUTYLAMMONIUM; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 77955686519     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.04.041     Document Type: Article
Times cited : (14)

References (78)
  • 48
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    • 3-iodanes
    • 3-iodanes, see:
  • 62
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    • For proton affinities of bromide and chloride anions
    • For proton affinities of bromide and chloride anions, see: S. Gronert J. Am. Chem. Soc. 115 1993 10258
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10258
    • Gronert, S.1
  • 69
    • 0001607830 scopus 로고    scopus 로고
    • For a vicinal steric interaction in nucleophilic vinylic substitutions of β-halostyrenes, see: X. Chen, and Z. Rappoport J. Org. Chem. 63 1998 5684
    • (1998) J. Org. Chem. , vol.63 , pp. 5684
    • Chen, X.1    Rappoport, Z.2
  • 70
    • 77955677982 scopus 로고    scopus 로고
    • Note
    • It is desirable to determine whether the close contacts (3.083, 3.131 ) between oxygen and iodine(III) atoms of (Z)- 4, being definitively shorter than the sum of the van der Waal's radii (3.5 ), are due to an attractive or repulsive interaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.