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Literature DB >> 21344578

Nickel-catalyzed amination of aryl sulfamates.

Stephen D Ramgren¹, Amanda L Silberstein, Yang Yang, Neil K Garg.

Abstract

Entities: Chemical Disease Gene

Mesh：

Substances：

Year: 2011 PMID： 21344578 PMCID： PMC3389547 DOI： 10.1002/anie.201007325

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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19 in total

1. Nickel-catalyzed cross-coupling of aryl grignard reagents with aromatic alkyl ethers: an efficient synthesis of unsymmetrical biaryls.

Authors: John W Dankwardt
Journal: Angew Chem Int Ed Engl Date: 2004-04-26 Impact factor: 15.336

2. Cross-coupling of aryl/alkenyl pivalates with organozinc reagents through nickel-catalyzed C-O bond activation under mild reaction conditions.

Authors: Bi-Jie Li; Yi-Zhou Li; Xing-Yu Lu; Jia Liu; Bing-Tao Guan; Zhang-Jie Shi
Journal: Angew Chem Int Ed Engl Date: 2008 Impact factor: 15.336

3. Exploring new uses for C-H amination: Ni-catalyzed cross-coupling of cyclic sulfamates.

Authors: Paul M Wehn; J Du Bois
Journal: Org Lett Date: 2005-10-13 Impact factor: 6.005

4. Nickel-catalyzed amination of aryl pivalates by the cleavage of aryl C-O bonds.

Authors: Toshiaki Shimasaki; Mamoru Tobisu; Naoto Chatani
Journal: Angew Chem Int Ed Engl Date: 2010-03-12 Impact factor: 15.336

5. Suzuki-Miyaura coupling of aryl carbamates, carbonates, and sulfamates.

Authors: Kyle W Quasdorf; Michelle Riener; Krastina V Petrova; Neil K Garg
Journal: J Am Chem Soc Date: 2009-12-16 Impact factor: 15.419

6. N,N-diethyl O-carbamate: directed metalation group and orthogonal Suzuki-Miyaura cross-coupling partner.

Authors: Aurora Antoft-Finch; Tom Blackburn; Victor Snieckus
Journal: J Am Chem Soc Date: 2009-12-16 Impact factor: 15.419

7. Nickel-catalyzed efficient and practical Suzuki-Miyaura coupling of alkenyl and aryl carbamates with aryl boroxines.

Authors: Li Xu; Bi-Jie Li; Zhen-Hua Wu; Xing-Yu Lu; Bing-Tao Guan; Bi-Qin Wang; Ke-Qing Zhao; Zhang-Jie Shi
Journal: Org Lett Date: 2010-02-19 Impact factor: 6.005

8. Nickel-catalyzed cross-coupling of aryl methyl ethers with aryl boronic esters.

Authors: Mamoru Tobisu; Toshiaki Shimasaki; Naoto Chatani
Journal: Angew Chem Int Ed Engl Date: 2008 Impact factor: 15.336

9. Cross-coupling reactions of aryl pivalates with boronic acids.

Authors: Kyle W Quasdorf; Xia Tian; Neil K Garg
Journal: J Am Chem Soc Date: 2008-10-08 Impact factor: 15.419

10. Nickel-catalyzed amination of aryl tosylates.

Authors: Cai-Yan Gao; Lian-Ming Yang
Journal: J Org Chem Date: 2008-01-17 Impact factor: 4.354

19 in total

1. Activation of C-O and C-N Bonds Using Non-Precious-Metal Catalysis.

Authors: Timothy B Boit; Ana S Bulger; Jacob E Dander; Neil K Garg
Journal: ACS Catal Date: 2020-09-10 Impact factor: 13.084

2. Breaking Amides using Nickel Catalysis.

Authors: Jacob E Dander; Neil K Garg
Journal: ACS Catal Date: 2017-01-06 Impact factor: 13.084

3. Cross-Coupling and Related Reactions: Connecting Past Success to the Development of New Reactions for the Future.

Authors: Louis-Charles Campeau; Nilay Hazari
Journal: Organometallics Date: 2018-11-27 Impact factor: 3.876

4. Mechanism and Origins of Ligand-Controlled Stereoselectivity of Ni-Catalyzed Suzuki-Miyaura Coupling with Benzylic Esters: A Computational Study.

Authors: Shuo-Qing Zhang; Buck L H Taylor; Chong-Lei Ji; Yuan Gao; Michael R Harris; Luke E Hanna; Elizabeth R Jarvo; K N Houk; Xin Hong
Journal: J Am Chem Soc Date: 2017-09-07 Impact factor: 15.419

5. Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.

Authors: Kyle W Quasdorf; Aurora Antoft-Finch; Peng Liu; Amanda L Silberstein; Anna Komaromi; Tom Blackburn; Stephen D Ramgren; K N Houk; Victor Snieckus; Neil K Garg
Journal: J Am Chem Soc Date: 2011-04-01 Impact factor: 15.419

6. C-N Cross-Coupling via Photoexcitation of Nickel-Amine Complexes.

Authors: Chern-Hooi Lim; Max Kudisch; Bin Liu; Garret M Miyake
Journal: J Am Chem Soc Date: 2018-06-11 Impact factor: 15.419

7. Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates.

Authors: Nathaniel H Park; Georgiy Teverovskiy; Stephen L Buchwald
Journal: Org Lett Date: 2013-11-27 Impact factor: 6.005