Organic chemist David A. Evans dies at 81 – Chemical & Engineering News

Already have an ACS ID?
This site uses cookies to enhance your user experience. By continuing to use this site you are agreeing to our COOKIE POLICY.

Renew your membership, and continue to enjoy these benefits.
 
ERROR 1
ERROR 1
ERROR 2
ERROR 2
ERROR 2
ERROR 2
ERROR 2
Password and Confirm password must match.
If you have an ACS member number, please enter it here so we can link this account to your membership. (optional)
ERROR 2
ACS values your privacy. By submitting your information, you are gaining access to C&EN and subscribing to our weekly newsletter. We use the information you provide to make your reading experience better, and we will never sell your data to third party members.
Already have an ACS ID?


Already an ACS Member?  
$160 Regular Members & Society Affiliates
$55 Graduate Students
$25 Undergraduate Students
ACS’s Premium Package gives you full access to C&EN and everything the ACS Community has to offer.
$80 Regular Members
ACS’s Standard Package lets you stay up to date with C&EN, stay active in ACS, and save.
$0 Community Associate

ACS’s Basic Package keeps you connected with C&EN and ACS.
Your account has been created successfully, and a confirmation email is on the way.
Your username is now your ACS ID.
Most Popular in People

 
David A. Evans, the Abbott and James Lawrence Professor Emeritus in the Department of Chemistry and Chemical Biology at Harvard University, died April 29 at the age of 81.
Former students and colleagues remember Evans as a dedicated educator and a creative force in organic synthesis. He is best known for devising a way to use chiral oxazolidinone auxiliaries to control a target molecule’s stereochemistry. “That changed the whole mindset of how people thought about going about building molecules stereoselectively,” says David W. C. MacMillan, a chemistry professor at Princeton University who worked with Evans as a postdoctoral fellow in the late 1990s. Before Evans’s work, chemists used a small number of building blocks known as the chiral pool. “When Dave came along, he upended all of that thinking,” MacMillan says.
Evans invented dozens of other useful synthetic methods, including sigmatropic rearrangements and hydride reductions. He also explored and made important contributions in the fields of organosilicon and organosulfur chemistry.
“I think people will remember not only the methodology but the impact of that methodology on total synthesis,” says Margaret Faul, who earned her PhD in Evans’s group in the early 1990s and is now vice president of manufacturing and clinical supply at Amgen. Evans’s synthetic strategies were used to make sublimely complex natural products, including the glycosylated antibiotic vancomycin and bryostatin 2, a marine macrolide lactone.
In addition to his contributions to chemistry, many remember Evans as a passionate teacher. He and his wife, Sally, also were involved in developing and popularizing the chemical structure–drawing software ChemDraw.
Evans was born in Washington, DC, in 1941. He studied chemistry with Norman Craig at Oberlin College and earned his bachelor’s degree in 1963. Evans completed his doctoral studies in 1967 at the California Institute of Technology, where he worked with Robert E. Ireland. He held faculty positions at the University of California, Los Angeles, and Caltech before moving to Harvard in 1983.
Evans garnered many honors during his career, including the American Chemical Society’s Arthur C. Cope Award, the Welch Award, and the Roger Adams Award in Organic Chemistry.
Donations in his memory can be made in support of Oberlin College’s David A. Evans ’63 Chemistry Prize at advance.oberlin.edu/donate.
Sign up for C&EN’s must-read weekly newsletter

Article:

This article has been sent to the following recipient:

Contact the reporter
Submit a Letter to the Editor for publication
Engage with us on Twitter
Sign up for C&EN’s must-read weekly newsletter
Copyright © 2022 American Chemical Society. All Rights Reserved.

source