efficient-synthesis-polyfunctionalized-benzenes-water-via-persulfate

Efficient Synthesis of Polyfunctionalized Benzenes in Water <em>via</em> Persulfate-promoted Benzannulation of &#945;,&#946;-Unsaturated Compounds and Alkynes

Benzannulation reactions represent an effective protocol to transform acyclic building blocks into structurally varied benzene skeletons. Despite ...

University of Campinas

The total synthesis of pteridic acids A and B is reported. The convergent asymmetric synthesis involved the use of a diastereoselective ethyl ketone aldol reaction followed by an efficient spiroketalization and provided pteridic acids A and B in 2.9% and 2.8% overall yield, respectively.

Airton G. Salles

Department of Organic Chemistry,
Institute of Chemistry,
Department of Organic Chemistry, Institute of Chemistry

University of Campinas

Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes

Airton G. Salles

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Department of Organic Chemistry,Institute of Chemistry,Department of Organic Chemistry, Institute of Chemistry

University of Campinas

Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes

Department of Organic Chemistry,
Institute of Chemistry,
Department of Organic Chemistry, Institute of Chemistry