UV, IR, AND PMR spectra of hydroxyhexamethylbenzenonium ions

Shubin, V. G.; Chzhu, V. P.; Korobeinicheva, I. K.; Rezvukhin, A. I.; Koptyug, V. A.

doi:10.1007/bf00996497

Russ Chem Bull

1970

DOI: 10.1007/bf00996497

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UV, IR, AND PMR spectra of hydroxyhexamethylbenzenonium ions

V. G. Shubin

V. P. Chzhu

I. K. Korobeinicheva

et al.

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1975

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Too many rearrangements of cyclohexadienones

Miller¹

1975

Acc. Chem. Res.

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Molecular rearrangements have long entranced the romantic spirits among organic chemists. While their colleagues plodded away, measuring minute rate differences and defining the structures of transition states for common reactions ever more precisely, students of molecular rearrangements raced ahead, hap-Bernard Miller received his Ph.D. from Columbia University, where he worked on free-radical halogenations, Finding these reactions insufficiently radical, he accepted a postdoctoral fellowship in steroid synthesis at the University of Wisconsin. This invaluable experience having taught him that his talents did not lie in natural product chemistry, he joined the American Cyanamid Co., synthesizing insecticides. Finding insects unexpectedly tough adversaries, he entered the academic life at the University of Massachusetts, where he is presently Professor of Chemistry. In addition to his research papers, he is the author of some 20 patents, none of which has ever increased his Income. His present research interests lie principally in the fields of molecular rearrangements and the reactions of blocked aromatic molecules.

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Too many rearrangements of cyclohexadienones

Miller¹

1975

Acc. Chem. Res.

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UV, IR, AND PMR spectra of hydroxyhexamethylbenzenonium ions

Cited by 1 publication

References 12 publications

Too many rearrangements of cyclohexadienones

Too many rearrangements of cyclohexadienones

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