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Volumn 61, Issue 4, 2005, Pages 747-789

Cyclic nitriles: Tactical advantages in synthesis

Author keywords

Cyanation; Cyclic nitriles; Stereoselectivity

Indexed keywords

ALKENE DERIVATIVE; NITRILE;

EID: 11044222000     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.11.012     Document Type: Review
Times cited : (109)

References (423)
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    • The stereochemical induction caused by the nitrile-substituent is unclear since analogous substitution in an intermolecular Diels-Alder cycloaddition does not appear to control the endo/exo selectivity: R. Grigg, R. Scott, and P. Stevenson J. Chem. Soc. Perkin Trans. 1 1988 1365
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    • Cyanation of α-alkoxy and α-amino nitriles are not surveyed, see: D. Enders, and J.P. Shilvock Chem. Soc. Rev. 29 2000 359
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    • note
    • The reaction is likely an E1cb elimination-conjugate addition.
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    • (f) Ref. 135
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    • For a discussion of inversion barrier and mechanism see: P.R. Carlier Chirality 15 2003 340
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    • note
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    • note
    • For a discussion of the structure of metallated nitriles see Ref. 21a.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.