Literature DB >> 19702329

Pt-catalyzed enantioselective diboration of terminal alkenes with B2(pin)2.

Laura T Kliman1, Scott N Mlynarski, James P Morken.   

Abstract

The Pt-catalyzed enantioselective addition of bis(pinacolato)diboron to simple monosubstituted alkenes is described. This reaction occurs in the presence of a readily available chiral phosphonite ligand and is effective with a variety of terminal alkene substrates. Importantly, the reaction can operate with catalyst loadings of only 1 mol % Pt. While oxidation of the intermediate 1,2-bis(boronate) ester provides the chiral 1,2-diol as the reaction product, the intermediate may also be subjected to homologation/oxidation to furnish a chiral 1,4-diol as the reaction product.

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Year:  2009        PMID: 19702329      PMCID: PMC2763309          DOI: 10.1021/ja9047762

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  15 in total

1.  Element-element additions to unsaturated carbon-carbon bonds catalyzed by transition metal complexes.

Authors:  Irina Beletskaya; Christina Moberg
Journal:  Chem Rev       Date:  2006-06       Impact factor: 60.622

2.  Unprecedented use of silver(I) N-heterocyclic carbene complexes for the catalytic preparation of 1,2-bis(boronate) esters.

Authors:  Jesus Ramírez; Rosa Corberán; Mercedes Sanaú; Eduardo Peris; Elena Fernandez
Journal:  Chem Commun (Camb)       Date:  2005-05-06       Impact factor: 6.222

3.  Platinum-catalyzed diboration using a commercially available catalyst: diboration of aldimines to alpha-aminoboronate esters

Authors: 
Journal:  Org Lett       Date:  2000-07-13       Impact factor: 6.005

4.  Direct boronation of allyl alcohols with diboronic acid using palladium pincer-complex catalysis. A remarkably facile allylic displacement of the hydroxy group under mild reaction conditions.

Authors:  Vilhelm J Olsson; Sara Sebelius; Nicklas Selander; Kalman J Szabó
Journal:  J Am Chem Soc       Date:  2006-04-12       Impact factor: 15.419

5.  Rh-catalyzed enantioselective diboration of simple alkenes: reaction development and substrate scope.

Authors:  Stéphane Trudeau; Jeremy B Morgan; Mohanish Shrestha; James P Morken
Journal:  J Org Chem       Date:  2005-11-11       Impact factor: 4.354

6.  Copper-catalyzed enantioselective substitution of allylic carbonates with diboron: an efficient route to optically active alpha-chiral allylboronates.

Authors:  Hajime Ito; Shinichiro Ito; Yusuke Sasaki; Kou Matsuura; Masaya Sawamura
Journal:  J Am Chem Soc       Date:  2007-11-08       Impact factor: 15.419

7.  Rhodium-catalyzed enantioselective diboration of simple alkenes.

Authors:  Jeremy B Morgan; Steven P Miller; James P Morken
Journal:  J Am Chem Soc       Date:  2003-07-23       Impact factor: 15.419

Review 8.  Catalytic enantioselective diboration, disilation and silaboration: new opportunities for asymmetric synthesis.

Authors:  Heather E Burks; James P Morken
Journal:  Chem Commun (Camb)       Date:  2007-08-22       Impact factor: 6.222

9.  Metal-catalyzed reactions of diborons for synthesis of organoboron compounds.

Authors:  Tatsuo Ishiyama; Norio Miyaura
Journal:  Chem Rec       Date:  2004       Impact factor: 6.771

10.  Catalytic asymmetric carbohydroxylation of alkenes by a tandem diboration/Suzuki cross-coupling/oxidation reaction.

Authors:  Steven P Miller; Jeremy B Morgan; Felix J Nepveux; James P Morken
Journal:  Org Lett       Date:  2004-01-08       Impact factor: 6.005

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  33 in total

1.  Catalytic enantioselective diboration of cyclic dienes. A modified ligand with general utility.

Authors:  Kai Hong; James P Morken
Journal:  J Org Chem       Date:  2011-09-20       Impact factor: 4.354

2.  Enantioselective 1,1-arylborylation of alkenes: merging chiral anion phase transfer with Pd catalysis.

Authors:  Hosea M Nelson; Brett D Williams; Javier Miró; F Dean Toste
Journal:  J Am Chem Soc       Date:  2015-02-27       Impact factor: 15.419

3.  Catalytic Enantioselective Synthesis of anti-Vicinal Silylboronates by Conjunctive Cross-Coupling.

Authors:  Yan Meng; Ziyin Kong; James P Morken
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-19       Impact factor: 15.336

4.  1,2-Boron Shifts of β-Boryl Radicals Generated from Bis-boronic Esters Using Photoredox Catalysis.

Authors:  Daniel Kaiser; Adam Noble; Valerio Fasano; Varinder K Aggarwal
Journal:  J Am Chem Soc       Date:  2019-09-03       Impact factor: 15.419

5.  Enantioselective synthesis of boron-substituted quaternary carbon stereogenic centers through NHC-catalyzed conjugate additions of (pinacolato)boron units to enones.

Authors:  Suttipol Radomkit; Amir H Hoveyda
Journal:  Angew Chem Int Ed Engl       Date:  2014-02-24       Impact factor: 15.336

6.  Enantioselective construction of all-carbon quaternary centers by branch-selective Pd-catalyzed allyl-allyl cross-coupling.

Authors:  Ping Zhang; Hai Le; Robert E Kyne; James P Morken
Journal:  J Am Chem Soc       Date:  2011-06-07       Impact factor: 15.419

7.  Atom-Economical Ni-Catalyzed Diborylative Cyclization of Enynes: Preparation of Unsymmetrical Diboronates.

Authors:  Natalia Cabrera-Lobera; M Teresa Quirós; William W Brennessel; Michael L Neidig; Elena Buñuel; Diego J Cárdenas
Journal:  Org Lett       Date:  2019-07-29       Impact factor: 6.005

8.  Catalytic enantioselective 1,2-diboration of 1,3-dienes: versatile reagents for stereoselective allylation.

Authors:  Laura T Kliman; Scott N Mlynarski; Grace E Ferris; James P Morken
Journal:  Angew Chem Int Ed Engl       Date:  2011-12-01       Impact factor: 15.336

9.  Vicinal diboronates in high enantiomeric purity through tandem site-selective NHC-Cu-catalyzed boron-copper additions to terminal alkynes.

Authors:  Yunmi Lee; Hwanjong Jang; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2009-12-30       Impact factor: 15.419

10.  Scope and mechanism of the Pt-catalyzed enantioselective diboration of monosubstituted alkenes.

Authors:  John R Coombs; Fredrik Haeffner; Laura T Kliman; James P Morken
Journal:  J Am Chem Soc       Date:  2013-07-18       Impact factor: 15.419

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