Angewandte Chemie(@angew_chem) 's Twitter Profile Photo

Copper(I)-Catalyzed Enantioconvergent Borylation of Racemic Benzyl Chlorides Enabled by Quadrant-by-Quadrant Structure Modification of Chiral Bisphosphine Ligands (Ito) doi.wiley.com/10.1002/anie.2…

Copper(I)-Catalyzed Enantioconvergent Borylation of Racemic Benzyl Chlorides Enabled by Quadrant-by-Quadrant Structure Modification of Chiral Bisphosphine Ligands (Ito) doi.wiley.com/10.1002/anie.2…
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Top Science(@isciverse) 's Twitter Profile Photo

Chiral Bisphosphine-Catalyzed Asymmetric Staudinger/aza-Wittig Reaction: An Enantioselective Desymmetrizing Approach to Crinine-Type Amaryllidaceae Alkaloids

J. Am. Chem. Soc.

pubs.acs.org/doi/10.1021/ja…

Chiral Bisphosphine-Catalyzed Asymmetric Staudinger/aza-Wittig Reaction: An Enantioselective Desymmetrizing Approach to Crinine-Type Amaryllidaceae Alkaloids

@J_A_C_S #Chemistry #Chemed #Science #TechnologyNews #news #technology #AcademicTwitter 

pubs.acs.org/doi/10.1021/ja…
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Chem. Asian J.(@ChemAsianJ) 's Twitter Profile Photo

Enantioselective Synthesis of Bromodifluoromethyl-containing Oxazolines by Concerted Lewis/Bronsted Base with Chiral Bisphosphine Oxide. Yoshitaka Hamashima et al. of University of Shizuoka onlinelibrary.wiley.com/doi/10.1002/as…

Enantioselective Synthesis of Bromodifluoromethyl-containing Oxazolines by Concerted Lewis/Bronsted Base #Catalysis with Chiral Bisphosphine Oxide. Yoshitaka Hamashima et al. of University of Shizuoka onlinelibrary.wiley.com/doi/10.1002/as…
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William Tolman(@WBTolman) 's Twitter Profile Photo

And here's issue 12! pubs.acs.org/toc/inocaj/55/…. Cover: computer-aided design of bisphosphine oxides for lanthanides

And here's issue 12! pubs.acs.org/toc/inocaj/55/…. Cover: computer-aided design of bisphosphine oxides for lanthanides
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Angewandte Chemie(@angew_chem) 's Twitter Profile Photo

M. Zhu, W. Zuo, etal. of Donghua University describe the diastereoselective synthesis of bisphosphine ligands combining both axial and P-centered chirality doi.wiley.com/10.1002/anie.2…

M. Zhu, W. Zuo, etal. of Donghua University describe the diastereoselective synthesis of bisphosphine ligands combining both axial and P-centered chirality doi.wiley.com/10.1002/anie.2…
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Angie R Angeles(@angierangeles) 's Twitter Profile Photo

Raphael Kim from ⁦DAWatsonLab⁩ ⁦Univ. of Delaware⁩ presented his graduate work ACS Organic Division 2021 GRS! Very nice talk Raphael on “Development of a Nickel-Catalyzed Atropselective Ullmann Coupling en route to Chiral Biaryl Bisphosphine Ligands”

Raphael Kim from ⁦@DAWatsonLab⁩            ⁦@UDelaware⁩ presented his graduate work @acsorganic 2021 GRS! Very nice talk Raphael on “Development of a Nickel-Catalyzed Atropselective Ullmann Coupling en route to Chiral Biaryl Bisphosphine Ligands” #GRS2021 #2021GRS
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PQI.org(@PGHQuantum) 's Twitter Profile Photo

'Application of Trimethylgermanyl-Substituted Bisphosphine Ligands with Enhanced Dispersion Interactions to Copper-Catalyzed Hydrobo-ration of Disubstituted Alkenes' by Y. Xi, B. Su, X. Qi, S. Pedram, P. Liu, and more!

Read more:
doi.org/10.1021/jacs.0…

'Application of Trimethylgermanyl-Substituted Bisphosphine Ligands with Enhanced Dispersion Interactions to Copper-Catalyzed Hydrobo-ration of Disubstituted Alkenes' by Y. Xi, B. Su, X. Qi, S. Pedram, P. Liu, and more! #pqi #publications

Read more:
doi.org/10.1021/jacs.0…
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Organic Process Research & Development(@OPRD_ACS) 's Twitter Profile Photo

Nippon Chemical team reports on the Rh-catalyzed asymmetric hydrogenation of alkenes with TON of up to 200 000 with a new, stable bulky three-hindered quadrant bisphosphine ligand, ee up to 99%; 30 examples J Org Chem/Org Lett .
pubs.acs.org/doi/10.1021/ac…

Nippon Chemical team reports on the Rh-catalyzed asymmetric hydrogenation of alkenes with TON of up to 200 000 with a new, stable bulky three-hindered quadrant bisphosphine ligand, ee up to 99%; 30 examples @JOC_OL . 
pubs.acs.org/doi/10.1021/ac…
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Chem. Asian J.(@ChemAsianJ) 's Twitter Profile Photo

Weak Electrostatic Interactions with Bisphosphine Ligands Facilitate Reductive Elimination of PhCF3 from Pd(II) Complexes. (Lu et al.) onlinelibrary.wiley.com/doi/10.1002/as…

Weak Electrostatic Interactions with Bisphosphine Ligands Facilitate Reductive Elimination of PhCF3 from Pd(II) Complexes. (Lu et al.) onlinelibrary.wiley.com/doi/10.1002/as…
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Organic Chemistry Portal(@organic_portal) 's Twitter Profile Photo

A chiral bisphosphine dioxide catalyzes an asymmetric conjugate reduction of acyclic β,β-disubstituted α,β-unsaturated ketones:
organic-chemistry.org/abstracts/lit6…

A chiral bisphosphine dioxide catalyzes an asymmetric conjugate reduction of acyclic β,β-disubstituted α,β-unsaturated ketones: 
organic-chemistry.org/abstracts/lit6…
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Organometallics(@Orgmet_ACS) 's Twitter Profile Photo

DFT Investigation: Ligand dissociation is avoided using Lewis acids in a bisphosphine cycle for Ni0/LA-catalyzed cyanoesterification bit.ly/2hYBMWe

DFT Investigation: Ligand dissociation is avoided using Lewis acids in a bisphosphine cycle for Ni0/LA-catalyzed cyanoesterification bit.ly/2hYBMWe
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Organic Chemistry Portal(@organic_portal) 's Twitter Profile Photo

organic-chemistry.org/abstracts/lit5…
A nickel/bisphosphine catalyst enables an asymmetric transfer hydrogenation of α,β-unsaturated esters

organic-chemistry.org/abstracts/lit5… 
A nickel/bisphosphine catalyst enables an asymmetric transfer hydrogenation of α,β-unsaturated esters
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J. Am. Chem. Soc.(@J_A_C_S) 's Twitter Profile Photo

From this week's front covers: 'Chiral Bisphosphine-Catalyzed Asymmetric Staudinger/aza-Wittig Reaction: An Enantioselective Desymmetrizing Approach to Crinine-Type Amaryllidaceae Alkaloids'.

Read the full article ➡️ go.acs.org/9xx

From this week's front covers: 'Chiral Bisphosphine-Catalyzed Asymmetric Staudinger/aza-Wittig Reaction: An Enantioselective Desymmetrizing Approach to Crinine-Type Amaryllidaceae Alkaloids'.

Read the full article ➡️ go.acs.org/9xx
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Ken Lo(@bhkenlo) 's Twitter Profile Photo

Cu(I) Complexes of Amide Functionalized Bisphosphine: Proximity Enhanced Metal–Ligand Cooperativity and Its Catalytic Advantage in C(sp3)–H Bond Activation of Unactivated Cycloalkanes pubs.acs.org/doi/10.1021/ac… Ramakrishnan, Balakrishna, & co-workers Inorganic Chemistry

Cu(I) Complexes of Amide Functionalized Bisphosphine: Proximity Enhanced Metal–Ligand Cooperativity and Its Catalytic Advantage in C(sp3)–H Bond Activation of Unactivated Cycloalkanes pubs.acs.org/doi/10.1021/ac… Ramakrishnan, Balakrishna, & co-workers @InorgChem #copper #catalysis
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Organic Chemistry Portal(@organic_portal) 's Twitter Profile Photo

organic-chemistry.org/abstracts/lit6…
A chiral bisphosphine dioxide catalyzes an asymmetric conjugate reduction of acyclic β,β-disubstituted α,β-unsaturated ketones

organic-chemistry.org/abstracts/lit6… 
A chiral bisphosphine dioxide catalyzes an asymmetric conjugate reduction of acyclic β,β-disubstituted α,β-unsaturated ketones
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Organic Chemistry Portal(@organic_portal) 's Twitter Profile Photo

organic-chemistry.org/abstracts/lit7…
An asymmetric homocoupling of ortho-(iodo)arylphosphine oxides and ortho-(iodo)arylphosphonates provides highly enantioenriched axially chiral bisphosphine oxides and bisphosphonates

organic-chemistry.org/abstracts/lit7… 
An asymmetric homocoupling of ortho-(iodo)arylphosphine oxides and ortho-(iodo)arylphosphonates provides highly enantioenriched axially chiral bisphosphine oxides and bisphosphonates
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Organic Chemistry Portal(@organic_portal) 's Twitter Profile Photo

organic-chemistry.org/abstracts/lit8…
A bench-stable alkyl bisphosphine Mn(I) complex catalyzes an additive-free Mn(I)-catalyzed dehydrogenative silylation of terminal alkenes.

organic-chemistry.org/abstracts/lit8… 
A bench-stable alkyl bisphosphine Mn(I) complex catalyzes an additive-free Mn(I)-catalyzed dehydrogenative silylation of terminal alkenes.
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Organic Chemistry Portal(@organic_portal) 's Twitter Profile Photo

organic-chemistry.org/abstracts/lit6…
A copper-based photoredox catalyst, bearing a tridentate carbazolide/bisphosphine ligand, that can be activated upon irradiation by blue LEDs, achieves the coupling of a range of primary carbamates with unactivated secondary alkyl bromides

organic-chemistry.org/abstracts/lit6… 
A copper-based photoredox catalyst, bearing a tridentate carbazolide/bisphosphine ligand, that can be activated upon irradiation by blue LEDs, achieves the coupling of a range of primary carbamates with unactivated secondary alkyl bromides
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Organic Chemistry Portal(@organic_portal) 's Twitter Profile Photo

organic-chemistry.org/abstracts/lit8…
The use of a bisphosphine ligand with a rigid backbone enables a copper-catalyzed regioselective Markovnikov 3,4-hydrosilylation of 2-substituted 1,3-dienes

organic-chemistry.org/abstracts/lit8… 
The use of a bisphosphine ligand with a rigid backbone enables a copper-catalyzed regioselective Markovnikov 3,4-hydrosilylation of 2-substituted 1,3-dienes
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