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Literature DB >> 21732594

Cross-coupling of mesylated phenol derivatives with potassium alkoxymethyltrifluoroborates.

Abstract

Cross-coupling of mesylated phenol derivatives with various potassium alkoxymethyltrifluoroborates has been achieved. The corresponding aryl and heteroaryl alkoxymethyl compounds have been obtained with equal facility with both electron-rich and electron-poor substituents on the activated alcohol.

Entities: Chemical Disease Gene

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Year: 2011 PMID： 21732594 PMCID： PMC3150460 DOI： 10.1021/ol201469r

Source DB: PubMed Journal: Org Lett ISSN： 1523-7052 Impact factor: 6.005

24 in total

Review 1. Biosynthesis of ethers: unusual or common natural events?

Authors: Pablo Domínguez de María; Robert W van Gemert; Adrie J J Straathof; Ulf Hanefeld
Journal: Nat Prod Rep Date: 2010-02-02 Impact factor: 13.423

2. A general palladium-catalyzed Suzuki-Miyaura coupling of aryl mesylates.

Authors: Chau Ming So; Chak Po Lau; Fuk Yee Kwong
Journal: Angew Chem Int Ed Engl Date: 2008 Impact factor: 15.336

Review 3. Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners.

Authors: Ranjan Jana; Tejas P Pathak; Matthew S Sigman
Journal: Chem Rev Date: 2011-02-14 Impact factor: 60.622

4. A versatile catalyst system for Suzuki-Miyaura cross-coupling reactions of C(sp(2))-tosylates and mesylates.

Authors: Brijesh Bhayana; Brett P Fors; Stephen L Buchwald
Journal: Org Lett Date: 2009-09-03 Impact factor: 6.005

5. A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids.

Authors: Tom Kinzel; Yong Zhang; Stephen L Buchwald
Journal: J Am Chem Soc Date: 2010-10-13 Impact factor: 15.419

2. Suzuki-Miyaura cross-coupling reactions of potassium Boc-protected aminomethyltrifluoroborate with aryl and hetaryl mesylates.

Authors: Gary A Molander; Inji Shin
Journal: Org Lett Date: 2012-05-31 Impact factor: 6.005

3. Pd-catalyzed Suzuki-Miyaura cross-coupling reactions between sulfamates and potassium Boc-protected aminomethyltrifluoroborates.

Authors: Gary A Molander; Inji Shin
Journal: Org Lett Date: 2013-05-06 Impact factor: 6.005

4. Suzuki-Miyaura cross-coupling of potassium alkoxyethyltrifluoroborates: access to aryl/heteroarylethyloxy motifs.

Authors: Nicolas Fleury-Brégeot; Marc Presset; Floriane Beaumard; Virginie Colombel; Daniel Oehlrich; Frederik Rombouts; Gary A Molander
Journal: J Org Chem Date: 2012-11-06 Impact factor: 4.354

4 in total

Cross-coupling of mesylated phenol derivatives with potassium alkoxymethyltrifluoroborates.

Review 1. Biosynthesis of ethers: unusual or common natural events?

2. A general palladium-catalyzed Suzuki-Miyaura coupling of aryl mesylates.

Review 3. Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners.

4. A versatile catalyst system for Suzuki-Miyaura cross-coupling reactions of C(sp(2))-tosylates and mesylates.

5. A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids.

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

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

8. Preparation of potassium alkoxymethyltrifluoroborates and their cross-coupling with aryl chlorides.

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

10. Mechanism of Ni-catalyzed selective C-O bond activation in cross-coupling of aryl esters.

1. Cross-coupling of mesylated phenol derivatives with potassium cyclopropyltrifluoroborate.

2. Suzuki-Miyaura cross-coupling reactions of potassium Boc-protected aminomethyltrifluoroborate with aryl and hetaryl mesylates.

3. Pd-catalyzed Suzuki-Miyaura cross-coupling reactions between sulfamates and potassium Boc-protected aminomethyltrifluoroborates.

4. Suzuki-Miyaura cross-coupling of potassium alkoxyethyltrifluoroborates: access to aryl/heteroarylethyloxy motifs.