Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Doering, William von

The second prediction raises a question. Are the relative contributions of A and C to the Cope TS fixed, or do their relative contributions vary with the number of radical stabilizing substituents and the carbons to which they are attached Professor William von Eggers Doering, who has arguably contributed more than any other experimentalist to the understanding of the Cope rearrangement, has formulated this question succinctly in terms of two adjectives that he invented. Is the Cope TS centauric or chameleonic [5] ... [Pg.860]

Woodward began his career as instructor at Harvard in autumn 1937 and remained there until he died. He is renowned for brilliant syntheses of natural products. With his first student, William von Eggers Doering, Woodward published in 1944 what was considered at the time the first total synthesis of quinine. He was an early advocate of instrumentation, developing useful rules for ultraviolet spectroscopy. The 28-year-old Woodward employed combustion calorimetry to successfully argue against Sir Robert Robinson s... [Pg.261]

In 1929, Hans Fischer (Germany 1881-1945) synthesized protoporphyrin (hemin, 26), and quinine (1) was synthesized in 1944 by Robert B. Woodward (United States 1917-1979) and William von E. Doering (United States 1917-). Hemin contains the unit found in hemoglobin, the oxygen-carrying component of blood, and quinine is an effective antimalarial drug. In 1951, Sir Robert... [Pg.9]

Quinine Robert B. Woodward and William von Eggers Doering synthesize quinine, which is used as an antimalarial. [Pg.2061]

The list of other individuals who contributed to the evolution of this book is long indeed. First, we would express our appreciation to the professors who contributed so much to our scientific education Professors Arnold Gilbert, M. L. Bryant, the late W. N. Pirkle and Alta Sproull, C. N. Jones, S. F. Clark, R. S. Drago (KWW) the late Dorothy Vaughn, the late David Marker, the late Calvin Vanderwerf, the late Ralph N. Adams, and Professors F. S. Rowland, A. Tulinsky, and William von E. Doering (RED) Professors R. O Connor, the late G. L. Baker, W. B. Cook, the late G. J. Hunt, the late A. E. Martell, and the late M. Passer (MLP) and Professors Richard Eisenberg, the late E Albert Cotton, the late John A. Osborn, and Dr. Jerry Unruh (GGS). [Pg.1181]

The structure of this complex molecule presents an extraordinary synthetic challenge and was accomplished in the early 1940s by R. B. Woodward and William von E. Doering. It s worth a look at this synthesis. It was not only an achievement of brilliance, but used many of the reactions whose mechanisms we have studied. [Pg.1025]

Additional pressure to find new sources arose during World War 2, when the cinchona plantations of Indonesia were no longer accessible. A synthetic route was finally devised in 1944 by William von Egg-ers Doering and Robert Woodward at Harvard. Improved approaches were devised by Milan Uskokovic s team at Hoffmann-La Roche in the USA (in 1970) and Gilbert Stork at Columbia University (in 2001), but none of these intricate and therefore uneconomical syntheses has replaced the natural source. Perhaps the reactions you have encountered in the preceding sections will inspire you to find a simple, economical procedure that, in common with so many other chemical... [Pg.172]

In support of the 6-membered transition state mechanism (28) for MPV reductions depicted in Scheme III, deuterium tracer studies by von Doering and Ash-ner (33,34), and by Williams and coworkers (35) show that the source of hydride transferred to the carbonyl substrate is indeed the carbinol carbon. Later data from Moulton, et al. (34), in 1961 did not preclude the existence of a non-... [Pg.125]


See other pages where Doering, William von is mentioned: [Pg.326]    [Pg.239]    [Pg.18]    [Pg.134]    [Pg.137]    [Pg.235]    [Pg.260]    [Pg.279]    [Pg.53]    [Pg.872]    [Pg.187]    [Pg.352]    [Pg.172]    [Pg.565]    [Pg.448]    [Pg.448]    [Pg.225]    [Pg.461]    [Pg.461]    [Pg.170]    [Pg.236]   
See also in sourсe #XX -- [ Pg.239 ]

See also in sourсe #XX -- [ Pg.134 , Pg.137 , Pg.235 , Pg.260 ]

See also in sourсe #XX -- [ Pg.172 ]




SEARCH



© 2024 chempedia.info