Microwave-assisted syntheses of regioisomerically pure bromorhodamine derivatives. Academic Article

abstract

• [structure: see text] Regioisomerically pure bromo-substituted rhodamine derivatives (bromorosamines) were prepared via microwave-accelerated condensation reactions followed by oxidation with chloranil. Reaction optimization was conveniently performed by monitoring UV absorptions attributed to the product.

authors

• Burgess, Kevin

published proceedings

• Org Lett

altmetric score

• 9

author list (cited authors)

• Jiao, G., Castro, J. C., Thoresen, L. H., & Burgess, K.

citation count

• 31

complete list of authors

• Jiao, Guan-Sheng||Castro, Juan C||Thoresen, Lars H||Burgess, Kevin

publication date

• October 2003

publisher

• American Chemical Society (ACS)  Publisher

published in

• Organic Letters  Journal

keywords

• Chloranil
• Hydrocarbons, Brominated
• Microwaves
• Rhodamines
• Spectrophotometry, Ultraviolet
• Stereoisomerism
• Temperature

PubMed Central ID

• 14507202

Digital Object Identifier (DOI)

• 10.1021/ol035327u

start page

• 3675

end page

• 3677

volume

• 5

issue

• 20

URL

• http://dx.doi.org/10.1021/ol035327u