ChemInform Abstract: Efficient Access to Multifunctional Trifluoromethyl Alcohols Through Base-Free Catalytic Asymmetric C-Bond Formation with Terminal Ynamides.

ChemInform ◽  
2016 ◽  
Vol 47 (26) ◽  
Author(s):  
Andrea M. Cook ◽  
Christian Wolf
Keyword(s):  
Bond Formation ◽  
Efficient Access ◽  
Catalytic Asymmetric

Recent Advances in C–Br Bond Formation

Synlett ◽  
2021 ◽  
Author(s):  
Ying-Yeung Yeung ◽  
Jonathan Wong
Keyword(s):  
Organic Synthesis ◽  
Aromatic Compounds ◽  
Bond Formation ◽  
Cross Coupling ◽  
Catalytic Site ◽  
Atom Transfer ◽  
Bond Forming ◽  
Recent Advances ◽  
Catalytic Asymmetric ◽  
Site Selective

AbstractOrganobromine compounds are extremely useful in organic synthesis. In this perspective, a focused discussion on some recent advancements in C–Br bond-forming reactions is presented.1 Introduction2 Selected Recent Advances2.1 Catalytic Asymmetric Bromopolycyclization of Olefinic Substrates2.2 Catalytic Asymmetric Intermolecular Bromination2.3 Some New Catalysts and Reagents for Bromination2.4 Catalytic Site-Selective Bromination of Aromatic Compounds2.5 sp3 C–H Bromination via Atom Transfer/Cross-Coupling3 Outlook

scholarly journals Copper-catalyzed tandem reaction of 2-alkynylanilines with benzoquinones: efficient access to 3-indolylquinones

RSC Advances ◽  
2018 ◽  
Vol 8 (39) ◽  
pp. 22122-22126 ◽  
Author(s):  
Raveendra Jillella ◽  
Chang Ho Oh
Keyword(s):  
Efficient Method ◽  
Bond Formation ◽  
Tandem Reaction ◽  
Efficient Access

Copper-catalyzed domino cyclization of 2-alkynylanilines followed by C–C bond formation with quinones is an efficient method of accessing 3-indolyl quinones.

DDQ-mediated regioselective C–S bond formation: efficient access to allylic sulfides

2018 ◽  
Vol 5 (21) ◽  
pp. 3158-3162 ◽  
Author(s):  
Chunsheng Li ◽  
Jianxiao Li ◽  
Chaowei Tan ◽  
Wanqing Wu ◽  
Huanfeng Jiang
Keyword(s):  
Bond Formation ◽  
Metal Free ◽  
Efficient Access

A novel metal-free dehydrocoupling approach for constructing allylic sulfides via oxidative allylic C–H functionalization with high atom- and step-economy has been developed.

scholarly journals Alcohol-Initiated Dediazoniation of Aryldiazonium Ions to Aryl Radicals: A Simple and Efficient Route to Arylboronates

2018 ◽  
Vol 42 (9) ◽  
pp. 481-485
Author(s):  
Xiulian Zhang ◽  
Zhicheng Zhang ◽  
Yongbin Xie ◽  
Yujie Jiang ◽  
Ruibo Xu ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Bond Formation ◽  
Single Electron ◽  
Single Electron Transfer ◽  
Aryl Radical ◽  
Radical Species ◽  
Aryl Radicals ◽  
Efficient Access ◽  
Efficient Route ◽  
Operational Simplicity

A simple and efficient access to arylboronates was achieved with methanol-initiated borylation of aryldiazonium salts. Reduction of aryldiazonium ions by single electron transfer from methanol affords aryl radical species, which undergo a subsequent C–B bond formation with bis(pinacolato)diboron. This highly practical borylation process, which can be carried out on the gram-scale, enjoys operational simplicity as well as mild and catalyst-free conditions.

scholarly journals Catalytic asymmetric carbon–carbon bond formation using alkenes as alkylmetal equivalents

2012 ◽  
Vol 4 (8) ◽  
pp. 649-654 ◽  
Author(s):  
Rebecca M. Maksymowicz ◽  
Philippe M. C. Roth ◽  
Stephen P. Fletcher
Keyword(s):  
Bond Formation ◽  
Carbon Bond ◽  
Carbon Carbon Bond ◽  
Catalytic Asymmetric ◽  
Asymmetric Carbon

scholarly journals Catalytic Asymmetric CN Bond Formation: Phosphine-Catalyzed Intra- and Intermolecular γ-Addition of Nitrogen Nucleophiles to Allenoates and Alkynoates

2013 ◽  
Vol 52 (9) ◽  
pp. 2525-2528 ◽  
Author(s):  
Rylan J. Lundgren ◽  
Ashraf Wilsily ◽  
Nicolas Marion ◽  
Cong Ma ◽  
Ying Kit Chung ◽  
...  
Keyword(s):  
Bond Formation ◽  
Catalytic Asymmetric ◽  
Nitrogen Nucleophiles

Catalytic Asymmetric Diarylphosphine Addition to α-Diazoesters for the Synthesis of P-Stereogenic Phosphinates via P*—N Bond Formation

2020 ◽  
Vol 85 (22) ◽  
pp. 14763-14771
Author(s):  
László B. Balázs ◽  
Yinhua Huang ◽  
Jasmina B. Khalikuzzaman ◽  
Yongxin Li ◽  
Sumod A. Pullarkat ◽  
...  
Keyword(s):  
Bond Formation ◽  
Catalytic Asymmetric

Catalytic asymmetric addition reactions leading to carbon-carbon bond formation: Phenyl and alkenyl transfer to aldehydes and alkynylation of α-imino esters

2006 ◽  
Vol 78 (2) ◽  
pp. 267-274 ◽  
Author(s):  
Jian-Xin Ji ◽  
Jing Wu ◽  
Lijin Xu ◽  
Chiu-Wing Yip ◽  
Kim Hung Lam ◽  
...  
Keyword(s):  
Bond Formation ◽  
Optically Active ◽  
Amino Acid Derivatives ◽  
Addition Reactions ◽  
Terminal Alkynes ◽  
Reaction Conditions ◽  
Carbon Carbon Bond ◽  
Catalytic Asymmetric ◽  
High Yields ◽  
Imino Esters

Optically active tertiary aminonaphthol ligands were obtained by a new, convenient procedure and were found to catalyze the enantioselective alkenyl and phenyl transfer to aldehydes in high yields and excellent enantiomeric excesses (ee's). The catalytic asymmetric introduction of alkynyl functionality to α-amino acid derivatives was realized by the direct addition of terminal alkynes to α-imino ester in the presence of chiral copper(I) complex under mild reaction conditions.

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