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Addition to olefins and acetylenes

Fahey, R. C., The Stereochemistry of Electrophilic Additions to Olefins and Acetylenes, 3, 237. Farina, M., The Stereochemistry of Linear Macromolecules, 17, 1. [Pg.596]

Electrophilic Additions to Olefins and Acetylenes, Stereochemistry of (Fahey) 3 237... [Pg.486]

O. R. XIII-3, C. Walling, and E. S. Huyser, Free Radical Additions to Olefins and Acetylenes to Form Carbon-Carbon Bonds XI11-1, G. Zweifel and H. C. Brown, Hydration of Olefins, Dienes, and Acetylenes via Hydroboration XIII-2, W. E. Parham and E. E. Schweizer, Halocyclopropanes from Halocarbenes. ... [Pg.1188]

S.7.2.3.3. by Addition to Olefins and Acetylenes or Cyclopropanes by Ring Opening. [Pg.365]

An alternative mechanism calls for hydrogen atom transfer by the reverse of eq 14 with no organome-tallic intermediates. Attempts to distinguish between these two possible pathways of hydrogen addition employed deuterium labeling. Stereoselectivity in the addition of LCoH to double and triple bonds was observed. Early work indicated Co—D cis addition to olefins and acetylenes.232 Later experiments showed... [Pg.531]

See other pages where Addition to olefins and acetylenes is mentioned: [Pg.302]    [Pg.594]    [Pg.1495]    [Pg.1495]    [Pg.237]    [Pg.251]    [Pg.214]    [Pg.367]    [Pg.369]    [Pg.371]    [Pg.375]    [Pg.377]    [Pg.381]    [Pg.383]    [Pg.385]    [Pg.387]    [Pg.389]    [Pg.340]    [Pg.334]    [Pg.61]    [Pg.63]    [Pg.82]    [Pg.83]    [Pg.85]    [Pg.93]    [Pg.97]    [Pg.105]    [Pg.109]    [Pg.119]    [Pg.121]    [Pg.123]    [Pg.125]    [Pg.131]   
See also in sourсe #XX -- [ Pg.137 ]



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Acetylenes addition

Addition to acetylenes

Additions to olefins

Electrophilic Additions to Olefins and Acetylenes, Stereochemistry of (Fahey)

Olefinic Acetylenes

Olefins, addition

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