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Activation of Small Molecules at N-Heterocyclic Carbene Centers
Activation of Small Molecules at N-Heterocyclic Carbene Centers
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Activation of Small Molecules at N-Heterocyclic Carbene Centers

Song, Hayoung ; Kim, Youngsuk ; Park, Junbeom ; Kim, Kimoon ; Lee, Eunsung

Synlett, 2016-03, Vol.27 (4), p.477-485 [Periódico revisado por pares]

Stuttgart · New York: Georg Thieme Verlag

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2
ANIPE-Cu Catalyst Enables Highly Enantioselective Markovnikov Hydroboration of α-Olefins
ANIPE-Cu Catalyst Enables Highly Enantioselective Markovnikov Hydroboration of α-Olefins
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ANIPE-Cu Catalyst Enables Highly Enantioselective Markovnikov Hydroboration of α-Olefins

Cai, Yuan ; Shi, Shi-Liang

Synlett, 2021-04, Vol.32 (6), p.545-550 [Periódico revisado por pares]

Rüdigerstraße 14, 70469 Stuttgart, Germany: Georg Thieme Verlag KG

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3
Rhodium-Catalyzed Reductive Cleavage of Aryl Carbamates Using Isopropanol as a Reductant
Rhodium-Catalyzed Reductive Cleavage of Aryl Carbamates Using Isopropanol as a Reductant
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Rhodium-Catalyzed Reductive Cleavage of Aryl Carbamates Using Isopropanol as a Reductant

Yasui, Kosuke ; Higashino, Masaya ; Chatani, Naoto ; Tobisu, Mamoru

Synlett, 2017-12, Vol.28 (19), p.2569-2572 [Periódico revisado por pares]

Stuttgart · New York: Georg Thieme Verlag

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4
ANIPE-Cu Catalyst Enables Highly Enantioselective Markovnikov Hydroboration of α-Olefins
ANIPE-Cu Catalyst Enables Highly Enantioselective Markovnikov Hydroboration of α-Olefins
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ANIPE-Cu Catalyst Enables Highly Enantioselective Markovnikov Hydroboration of α-Olefins

Cai, Yuan ; Shi, Shi-Liang

Synlett, 2020-11 [Periódico revisado por pares]

Rüdigerstraße 14, 70469 Stuttgart, Germany: Georg Thieme Verlag KG

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5
Total Synthesis of (+)-Tanikolide by a Traceless Stereoinduction Method Using Rhodium(II)-Catalyzed Oxonium Ylide Formation–[2,3]-Sigmatropic Rearrangement and NHC-Catalyzed Ring-Expansion Lactonization
Total Synthesis of (+)-Tanikolide by a Traceless Stereoinduction Method Using Rhodium(II)-Catalyzed Oxonium Ylide Formation–[2,3]-Sigmatropic Rearrangement and NHC-Catalyzed Ring-Expansion Lactonization
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Total Synthesis of (+)-Tanikolide by a Traceless Stereoinduction Method Using Rhodium(II)-Catalyzed Oxonium Ylide Formation–[2,3]-Sigmatropic Rearrangement and NHC-Catalyzed Ring-Expansion Lactonization

Nambu, Hisanori ; Jinnouchi, Hikari ; Fujiwara, Tomoya ; Yakura, Takayuki

Synlett, 2016-01, Vol.27 (7), p.1106-1009 [Periódico revisado por pares]

Stuttgart · New York: Georg Thieme Verlag

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6
Highly Regioselective Heck Coupling Reactions of Aryl Halides and Dihydropyran in the Presence of an NHC-Pyridine Ligand
Highly Regioselective Heck Coupling Reactions of Aryl Halides and Dihydropyran in the Presence of an NHC-Pyridine Ligand
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Highly Regioselective Heck Coupling Reactions of Aryl Halides and Dihydropyran in the Presence of an NHC-Pyridine Ligand

Jarusiewicz, Jamie ; Yoo, Kyung Soo ; Jung, Kyung Woon

Synlett, 2009-02, Vol.2009 (3), p.482-486 [Periódico revisado por pares]

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