Back to Results
First PageMeta Content
Allylic strain / Stereoselectivity / Ene reaction / Alkene / Singlet oxygen / Substituent / Photooxygenation / Chemistry / Stereochemistry / Organic reactions


The Reaction of Singlet Oxygen with Enecarbamates: A Mechanistic Playground for Investigating Chemoselectivity, Stereoselectivity, and Vibratioselectivity of Photooxidations J. SIVAGURU,*,† MARISSA R. SOLOMON,‡ THOMA
Add to Reading List

Document Date: 2008-06-01 13:24:22

Open Document

File Size: 2,10 MB

Share Result on Facebook

City

Würzburg / Claremont / Fargo / /

Company

GC / /

Country

Germany / /

Currency

USD / /

Facility

Institute für Organische Chemie / Columbia University / North Dakota State University / University of Puerto Rico / /

IndustryTerm

ene-products / ene product / enecarbamate cleavage product / dioxetane product / cycloaddition product / dioxetane cleavage product / chemical correlation / oxazolidinone carbonyl / /

Organization

§Joint Science Department / Universität Würzburg / W.M. Keck Science Center / North Dakota State University / University of Puerto Rico / Department of Chemistry and Molecular Biology / Columbia University / New York / Department of Chemistry / /

Person

MARISSA R. SOLOMON / Gq / STEFFEN JOCKUSCH / THOMAS POON / NICHOLAS J. TURRO / SARA G. BOSIO / Facundo Bueso / Mode Selectivity (Chemoselectivity) / /

Position

stereochemical reporter / RT / Representative / /

Product

C-4R E-1i / C-3 / 1O2 / /

ProgrammingLanguage

R / /

ProvinceOrState

North Dakota / California / New York / /

PublishedMedium

ACCOUNTS OF CHEMICAL RESEARCH / Molecular Biology / /

Technology

X-ray / spectroscopy / /

URL

www.pubs.acs.org/acr / /

SocialTag