The Experts below are selected from a list of 267 Experts worldwide ranked by ideXlab platform
Keisuke Fukuhara - One of the best experts on this subject based on the ideXlab platform.
-
Rhodium-Catalyzed Addition—Spirocyclization of Arylboronic Esters Containing β-Aryl α,β-Unsaturated Ester Moiety.
ChemInform, 2015Co-Authors: Takanori Matsuda, Satoshi Yasuoka, Shoichi Watanuki, Keisuke FukuharaAbstract:Spirocyclic 1-indanones are synthesized by rhodium-catalyzed spirocyclization involving sequential transmetalation, intramolecular addition to a C=C bond, and β-oxygen elimination.
-
rhodium catalyzed addition spirocyclization of arylboronic Esters containing β aryl α β unsaturated Ester moiety
Synlett, 2015Co-Authors: Takanori Matsuda, Satoshi Yasuoka, Shoichi Watanuki, Keisuke FukuharaAbstract:In this study, we developed a rhodium(I)-catalyzed spirocyclization. The reaction includes 1,4-rhodium migration and provides a route for forming spirocyclic 1-indanones.
Takanori Matsuda - One of the best experts on this subject based on the ideXlab platform.
-
Rhodium-Catalyzed Addition—Spirocyclization of Arylboronic Esters Containing β-Aryl α,β-Unsaturated Ester Moiety.
ChemInform, 2015Co-Authors: Takanori Matsuda, Satoshi Yasuoka, Shoichi Watanuki, Keisuke FukuharaAbstract:Spirocyclic 1-indanones are synthesized by rhodium-catalyzed spirocyclization involving sequential transmetalation, intramolecular addition to a C=C bond, and β-oxygen elimination.
-
rhodium catalyzed addition spirocyclization of arylboronic Esters containing β aryl α β unsaturated Ester moiety
Synlett, 2015Co-Authors: Takanori Matsuda, Satoshi Yasuoka, Shoichi Watanuki, Keisuke FukuharaAbstract:In this study, we developed a rhodium(I)-catalyzed spirocyclization. The reaction includes 1,4-rhodium migration and provides a route for forming spirocyclic 1-indanones.
Satoshi Yasuoka - One of the best experts on this subject based on the ideXlab platform.
-
Rhodium-Catalyzed Addition—Spirocyclization of Arylboronic Esters Containing β-Aryl α,β-Unsaturated Ester Moiety.
ChemInform, 2015Co-Authors: Takanori Matsuda, Satoshi Yasuoka, Shoichi Watanuki, Keisuke FukuharaAbstract:Spirocyclic 1-indanones are synthesized by rhodium-catalyzed spirocyclization involving sequential transmetalation, intramolecular addition to a C=C bond, and β-oxygen elimination.
-
rhodium catalyzed addition spirocyclization of arylboronic Esters containing β aryl α β unsaturated Ester moiety
Synlett, 2015Co-Authors: Takanori Matsuda, Satoshi Yasuoka, Shoichi Watanuki, Keisuke FukuharaAbstract:In this study, we developed a rhodium(I)-catalyzed spirocyclization. The reaction includes 1,4-rhodium migration and provides a route for forming spirocyclic 1-indanones.
Shoichi Watanuki - One of the best experts on this subject based on the ideXlab platform.
-
Rhodium-Catalyzed Addition—Spirocyclization of Arylboronic Esters Containing β-Aryl α,β-Unsaturated Ester Moiety.
ChemInform, 2015Co-Authors: Takanori Matsuda, Satoshi Yasuoka, Shoichi Watanuki, Keisuke FukuharaAbstract:Spirocyclic 1-indanones are synthesized by rhodium-catalyzed spirocyclization involving sequential transmetalation, intramolecular addition to a C=C bond, and β-oxygen elimination.
-
rhodium catalyzed addition spirocyclization of arylboronic Esters containing β aryl α β unsaturated Ester moiety
Synlett, 2015Co-Authors: Takanori Matsuda, Satoshi Yasuoka, Shoichi Watanuki, Keisuke FukuharaAbstract:In this study, we developed a rhodium(I)-catalyzed spirocyclization. The reaction includes 1,4-rhodium migration and provides a route for forming spirocyclic 1-indanones.
Duncan Bruce Judd - One of the best experts on this subject based on the ideXlab platform.
-
pentafluorophenyl sulfonate Ester as a protecting group for the preparation of biaryl and heterobiaryl sulfonate Esters
Organic Letters, 2005Co-Authors: Barbara G Avitabile, Clive A Smith, Duncan Bruce JuddAbstract:The use of the pentafluorophenyl (PFP) group as a sulfonic acid protecting group has allowed the synthesis of new biaryl- and heterobiaryl-PFP-sulfonate Esters by use of the Suzuki−Miyaura reaction. The successful employment of a novel inorganic base, anhydrous sodium tetraborate, was crucial to give the products in excellent yields. The PFP-sulfonate Ester has been previously shown to be an excellent alternative to sulfonyl chlorides in the synthesis of sulfonamides.
