Search Results - "Werner, Erik W"

Imparting Catalyst Control upon Classical Palladium-Catalyzed Alkenyl C–H Bond Functionalization Reactions by Sigman, Matthew S, Werner, Erik W

“…The functional group transformations carried out by the palladium-catalyzed Wacker and Heck reactions are radically different, but they are both alkenyl C–H…”
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Enantioselective Heck Arylations of Acyclic Alkenyl Alcohols Using a Redox-Relay Strategy by Werner, Erik W., Mei, Tian-Sheng, Burckle, Alexander J., Sigman, Matthew S.

“…Progress in the development of asymmetric Heck couplings of arenes and acyclic olefins has been limited by a tenuous understanding of the factors that dictate…”
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Total Synthesis of Dixiamycin B by Electrochemical Oxidation by Rosen, Brandon R, Werner, Erik W, O’Brien, Alexander G, Baran, Phil S

“…N–N-linked dimeric indole alkaloids represent an unexplored class of natural products for which chemical synthesis has no practical solution. To meet this…”
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Enantioselective Redox-Relay Oxidative Heck Arylations of Acyclic Alkenyl Alcohols using Boronic Acids by Mei, Tian-Sheng, Werner, Erik W, Burckle, Alexander J, Sigman, Matthew S

“…A general, highly selective asymmetric redox-relay oxidative Heck reaction using achiral or racemic acyclic alkenols and boronic acid derivatives is reported…”
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Operationally Simple and Highly (E)-Styrenyl-Selective Heck Reactions of Electronically Nonbiased Olefins by Werner, Erik W, Sigman, Matthew S

“…Simple, mild, and efficient conditions are reported for a Pd0-catalyzed Heck reaction that delivers high yields and selectivity for (E)-styrenyl products using…”
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A Highly Selective and General Palladium Catalyst for the Oxidative Heck Reaction of Electronically Nonbiased Olefins by Werner, Erik W, Sigman, Matthew S

“…A general, highly selective oxidative Heck reaction is reported. The reaction is high-yielding under mild conditions without the need for base or high…”
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Scalable, Enantioselective Synthesis of Germacrenes and Related Sesquiterpenes Inspired by Terpene Cyclase Phase Logic by Foo, Klement, Usui, Ippei, Götz, Daniel C. G., Werner, Erik W., Holte, Dane, Baran, Phil S.

“…Terpene cyclase phase: Inspired by this logic, a scalable and enantioselective divergent synthesis of germacrane‐type sesquiterpenes is developed. Salient…”
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PdII-Catalyzed Oxidative 1,1-Diarylation of Terminal Olefins by Werner, Erik W, Urkalan, Kaveri B, Sigman, Matthew S

“…Evaluation of the scope of a PdII-catalyzed oxidative 1,1-diarylation reaction of terminal olefins using aryl stannanes is reported. The reaction is shown to…”
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Pd(II)-catalyzed oxidative 1,1-diarylation of terminal olefins by Werner, Erik W, Urkalan, Kaveri B, Sigman, Matthew S

“…Evaluation of the scope of a Pd(II)-catalyzed oxidative 1,1-diarylation reaction of terminal olefins using aryl stannanes is reported. The reaction is shown to…”
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Scalable, Enantioselective Synthesis of Germacrenes and Related Sesquiterpenes Inspired by Terpene Cyclase Phase Logic by Foo, Klement, Usui, Ippei, Götz, Daniel C. G., Werner, Erik W., Holte, Dane, Baran, Phil S.

“…Terpen‐Zyklasenphase: Eine skalierbare und enantioselektive divergente Synthese von Germacran‐artigen Sesquiterpenen wurde entwickelt. Die besonderen Merkmale…”
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Operationally Simple and Highly (E)-Styrenyl-Selective Heck Reactions of Electronically Non-Biased Olefins by Werner, Erik W., Sigman, Matthew S.

“…Simple, mild, and efficient conditions are reported for a Pd 0 -catalyzed Heck reaction that delivers high yields and selectivity for (E) -styrenyl products…”
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Pd II -Catalyzed Oxidative 1,1-Diarylation of Terminal Olefins by Werner, Erik W., Urkalan, Kaveri B., Sigman, Matthew S.

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A Highly Selective and General Palladium Catalyst for the Oxidative Heck Reaction of Electronically Non-Biased Olefins by Werner, Erik W., Sigman, Matthew S.

“…A general, highly selective oxidative Heck reaction is reported. The reaction is high yielding under mild conditions without the need for base or high…”
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Enantioselective Heck Arylations of Acyclic Alkenyl Alcoholsx Using a Redox-Relay Strategy by Werner, Erik W., Mei, Tian-Sheng, Burckle, Alexander J., Sigman, Matthew S.

“…Progress in the development of asymmetric Heck couplings of arenes and acyclic olefins has been limited by a tenuous understanding of the factors that dictate…”
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