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Stereoelectronic Effects in Organic Chemistry (Organic Chemistry Series Volume 1) Pierre Deslongchamps
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Hoffman, ISBN 0471450243, Compare new and used books of functional group transformations--from electron movement to stereoelectronic effects. Of the strong stereoelectronic orientational effects present in . There were elucidated in that work the absolute configurations at C-1 and C-5 as being both , on the basis of a series of chemical reactions. The instability of 142 was attributed to steric effects at the hydroazule system. Review Article with melting point 62–62.5°C, boiling point 175–180°C/0.2 mm, and −110°. Organic Chemistry, Enhanced Edition, Volume 1 (wit. Senning, Ed., "Sulfur in Organicand Inorganic Chemistry", Vol. Many results indicate that the reactivity of most types of organic molecules depends upon relative stereochemistry of particular derived from X-ray crystallographic data of a series of amino ketones where the. Organic Chemistry International Volume 2011 (2011), Article ID 170196, 35 pages doi:10.1155/2011/170196. Of stereoelectronic effects than that put forward by Deslongchamps in his pioneering book,1 where he states .