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Mislow, Kurt

Mislow, Kurt, and Paul Bickart. "An Epistemological Note on Chirality." Israel Journal of Chemistry, 15 (19761977) 16. [Pg.333]

Roald Hoffmann, personal correspondence, letter of October 16, 1990. Also, R. Hoffmann, "Nearly Circular Reasoning," American Scientist, 76 (1988) 182185. And see Kurt Mislow and Paul Bickart, "An Epistemological Note on Chirality," Israel Journal of Chemistry 15 (197677) 16 "Thus chiral and achiral are used with two different connotations When the terms are applied to a geometric model, they are sharply defined, whereas when used in conjunction with observables, they necessarily entail a certain fuzziness" (6). [Pg.294]

KURT MISLOW, Princeton University, Princeton, New Jersey... [Pg.346]

Many of the ideas and examples in Chapter 1 have been extracted from notes of a course given by Kurt Mislow to a class of Princeton graduate students in 1968. [Pg.314]

I wish to express my thanks to Kurt Mislow and Corinne Cerf who each read a preliminary version of this chapter and gave me valuable suggestions. [Pg.34]

Prof. Dr. Kurt Mislow, Devens Gust, Dr. Paolo Finocchiaro and Dr. Robert J. Boettcher ... [Pg.1]

Stereochemistry continues to be a highly viable and prolific subject. Nonetheless, in 1993 the editors reluctantly decided to retire after publication of Volume 21, in part because for some time prior they had been fully occupied with the publication of Stereochemistry of Organic Compounds (Wiley, 1994). Sadly, my close friend, able coauthor and coeditor, and valued colleague Sam Wilen died soon thereafter. In as much as the explosive development in stereochemistry is continuing, I am delighted that Scott Denmark, who is eminently qualified for the task, has taken over editorship of the series with Volume 22.1 am particularly pleased to see a chapter by my fellow stereochemist Kurt Mislow in this volume, since Kurt helped us launch the series in 1967 by agreeing to be an editorial advisor and by coauthoring a seminal chapter on stereochemical relationships (heterotopicity) for... [Pg.325]

Figure 2-48. Reverse la coup du roi and the formation of dimer from two homochiral 4-(bromomethyl)-6-(mercaptomethyl) [2.2]metacyclophane molecules. After Anet et al. [78], Reprinted with permission from 1983 American Chemical Society and Kurt Mislow. Figure 2-48. Reverse la coup du roi and the formation of dimer from two homochiral 4-(bromomethyl)-6-(mercaptomethyl) [2.2]metacyclophane molecules. After Anet et al. [78], Reprinted with permission from 1983 American Chemical Society and Kurt Mislow.
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See also in sourсe #XX -- [ Pg.281 ]



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