G
George M. Whitesides
Researcher at Harvard University
Publications - 1754
Citations - 287794
George M. Whitesides is an academic researcher from Harvard University. The author has contributed to research in topics: Monolayer & Self-assembled monolayer. The author has an hindex of 240, co-authored 1739 publications receiving 269833 citations. Previous affiliations of George M. Whitesides include University of California, Davis & University of Texas at Austin.
Papers
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Journal ArticleDOI
Mechanism of reaction of carbon monoxide with phenyllithium
Larry S. Trzupek,Terry L. Newirth,Terry L. Newirth,Edward G. Kelly,Norma Ethyl Sbarbati,George M. Whitesides +5 more
TL;DR: The product mixtures obtained by reaction between phenyllithium and carbon monoxide in diethyl ether, followed by hydrolysis, include benzophenone (1), benzil (3), a,a-diphenyl- a-hydroxyacetophenone(4), benzpinacot (5), a-h-acetophenylophenone (6), 1,3,3-triphenylpropane-1,2-dione (7), 1.5, and benzhydrol (9).
Journal ArticleDOI
Crystals of crystals: fabrication of encapsulated and ordered two-dimensional arrays of microcrystals.
TL;DR: A new technique-crystallization in asymmetric microwells-generates arrays of small crystals with controlled size, orientation, and arrangement in space that can be generated in a form completely encapsulated in polymer.
Journal ArticleDOI
Shadowed sputtering of gold on V -shaped microtrenches etched in silicon and applications in microfabrication
Younan Xia,George M. Whitesides +1 more
Journal ArticleDOI
Polymer-based mesh as supports for multi-layered 3D cell culture and assays
Karen A. Simon,Kyeng Min Park,Bobak Mosadegh,Bobak Mosadegh,Anand Bala Subramaniam,Aaron D. Mazzeo,Philip M. Ngo,George M. Whitesides,George M. Whitesides +8 more
TL;DR: CiGiM simplifies the generation and analysis of 3D culture without compromising throughput, and quality of the data collected: it is especially useful in experiments that require control of oxygen levels, and isolation of adjacent wells in a multi-zone format.
Book ChapterDOI
Reagents for Rapid Reduction of Disulfide Bonds
TL;DR: This chapter describes the reagents that reduce disulfide bonds, under nondenaturing conditions at pH 7, faster than does dithiothreitol (DTT) by a factor of ∼5–7.8.