Sigma-Aldrich

Application 5-Bromopyridin-3-yl sulfurofluoridate can be used in the Pd-catalyzed Suzuki-Miyuara cross-coupling reaction. The fluorosulfate functionality was shown by Sharpless and coworkers to have distinct reactivity in comparison to other

Application 2-Bromopyridin-3-yl sulfurofluoridate can be used in the Pd-catalyzed Suzuki-Miyuara cross-coupling reaction. The fluorosulfate functionality was shown by Sharpless and coworkers to have distinct reactivity in comparison to other

Application The following spring-loaded" electrophile is a convenient reagent for the installation of cyclopentane to primary and secondary amines. This product is one of several synthetically useful reagents reported by Baran and coworkers for"

Application The following spring-loaded" electrophile is a convenient reagent for the installation of cyclopentane to primary and secondary amines. This product is one of several synthetically useful reagents reported by Baran and coworkers on"

1-((3,5-Difluorophenyl)sulfonyl)bicyclo[1.1.

5-Methoxy-1,2,3-triazine is a 1,2,3-triazine derivative bearing electron-donating substituent. It participates in the inverse electron demand Diels-Alder reactions.

Application The following Baran Sulfinate is a part of a toolbox of diversification reagents, which are ideal for the late-stage functionalization of nitrogen-containing heterocycles. The regioselectivity can be effectively tuned by modification of

Application The following Baran Sulfinate is a part of a toolbox of diversification reagents, which are ideal for the late-stage functionalization of nitrogen-containing heterocycles. The regioselectivity can be effectively tuned by modification of

Sodium (4-chlorophenyl)methanesulfinate is an alkyl Baran Diversinate. These reagents facilitate the functionalization of heteroaromatic C-H bonds under simple reaction conditions.

Sodium (2,4-dichlorophenyl)methanesulfinate is an alkyl baran diversinate. These reagents facilitate the functionalization of heteroaromatic C-H bonds under simple reaction conditions.

Application The following Baran Sulfinate is a part of a toolbox of diversification reagents, which are ideal for the late-stage functionalization of nitrogen-containing heterocycles. The regioselectivity can be effectively tuned by modification of

Application The following Baran Sulfinate is a part of a toolbox of diversification reagents, which are ideal for the late-stage functionalization of nitrogen-containing heterocycles. The regioselectivity can be effectively tuned by modification of