Skip To Main Content
Barry M. Trost on Muck Rack

Barry M. Trost

As seen in: Color Research & Application, Nature, ACS Publications, Analytical Chemistry, Science Magazine, Royal Society of Chemistry, Chemistry World
Is this you? As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work. Claim your profile

Get in touch with Barry M.

Contact Barry M., search articles and posts on X, monitor coverage, and track replies from one place.

Learn more about Muck Rack

Actions

Share this page

Is this you?

As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
Claim your profile

Articles

Total Synthesis of Kadcoccinic Acid A Trimethyl Ester

|
By Barry M. Trost, Guoting Zhang, Hadi Gholami, Daniel Zell
| ACS Publications
Download Hi-Res ImageDownload to MS-PowerPointCite This:J. Am. Chem. Soc. 2021, XXXX, XXX RETURN TO ARTICLES ASAPPREVArticleNEXT Barry M. Trost*, Guoting Zhang, Hadi Gholami, and Daniel Zell LEARN ABOUT THESE METRICS Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.
Open in Who Shared Issue with article?

Palladium-Catalyzed Asymmetric Allylic Alkylation (AAA) with Alkyl Sulfones as Nucleophiles

|
By Barry M. Trost, Zhiwei Jiao, Hadi Gholami
| Royal Society of Chemistry Verified
This article is Open Access Please wait while we load your content... Something went wrong. Try again?
Open in Who Shared View Duplicates (650) Issue with article?

Regiodivergent Synthesis of Spirocyclic Compounds through Pd‐Catalyzed Regio‐ and Enantioselective [3+2] Spiroannulation

|
By Barry M. Trost, Zhijun Zuo
| Color Research & Application Verified
Communication PDF ShareShare Abstract A novel Pd0‐catalyzed highly regio‐ and enantioselective [3+2] spiroannulation reaction has been developed for rapid assembly of a new class of [5,5] spirocyclic carbo‐ and heterocycles. Notably, the regioselectivity could be dominated by fine‐tuning of the Pd‐π‐allyl intermediate. An array of coupling partners could be well‐tolerated with excellent regio‐, and enantioselectivities.
Open in Who Shared Issue with article?
See all 45 articles