Generation and reactivity of the chiral rhenium chlorobenzene complex [(η5-C5H5)Re(NO)(PPh3)(ClC6H5)]+BF−4: an improved functional equivalent of the chiral Lewis acid [(η5-C5H5)Re(NO)(PPh3)]+BF−4

Journal of Organometallic Chemistry ◽

10.1016/0022-328x(90)85333-t ◽

1990 ◽

Vol 397 (3) ◽

pp. 333-346 ◽

Author(s):

James J. Kowalczyk ◽

Sénamé K. Agbossou ◽

J.A. Gladysz

Keyword(s):

Chiral Lewis Acid ◽

Functional Equivalent

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Theoretical investigation of dichloromethane ligand substitution in [(η5-C5H5)Re(NO)(PPh3)(ClCH2Cl)]+, a functional equivalent of a chiral Lewis acid

10.1021/scimeetings.1c00239 ◽

2021 ◽

Author(s):

Taveechai Wititsuwannakul ◽

Michael Hall ◽

John Gladysz

Keyword(s):

Theoretical Investigation ◽

Ligand Substitution ◽

Chiral Lewis Acid ◽

Functional Equivalent

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Computational Investigation of Dichloromethane Ligand Substitution in the Enantiopure Cation [(η5-C5H5)Re(NO)(PPh3)(ClCH2Cl)]+, a Functional Equivalent of a Chiral Lewis Acid

Organometallics ◽

10.1021/acs.organomet.1c00006 ◽

2021 ◽

Vol 40 (6) ◽

pp. 742-759

Author(s):

Taveechai Wititsuwannakul ◽

Michael B. Hall ◽

John A. Gladysz

Keyword(s):

Ligand Substitution ◽

Computational Investigation ◽

Chiral Lewis Acid ◽

Functional Equivalent

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Asymmetric synthesis of isoquinuclidines by Diels–Alder reaction of 1,2-dihydropyridine utilizing a chiral Lewis acid catalyst

Tetrahedron ◽

10.1016/j.tet.2011.12.041 ◽

2012 ◽

Vol 68 (6) ◽

pp. 1774-1781 ◽

Author(s):

Chigusa Seki ◽

Masafumi Hirama ◽

N.D.M. Romauli Hutabarat ◽

Junko Takada ◽

Chonticha Suttibut ◽

...

Keyword(s):

Asymmetric Synthesis ◽

Acid Catalyst ◽

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Chiral Lewis Acid ◽

Lewis Acid Catalyst

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Chiral Lewis Acid Catalysis in Nitrile Oxide Cycloadditions

Journal of the American Chemical Society ◽

10.1021/ja0318636 ◽

2004 ◽

Vol 126 (17) ◽

pp. 5366-5367 ◽

Author(s):

Mukund P. Sibi ◽

Kennosuke Itoh ◽

Craig P. Jasperse

Keyword(s):

Acid Catalysis ◽

Nitrile Oxide ◽

Lewis Acid Catalysis ◽

Chiral Lewis Acid

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Chiral Lewis Acid Controlled Synthesis (CLAC Synthesis): Chiral Lewis Acids Influence the Reaction Course in Asymmetric Aldol Reactions for the Synthesis of Enantiomeric Dihydroxythioester Derivatives in the Presence of Chiral Diamines Derived from L-Proline

Chemistry - A European Journal ◽

10.1002/chem.19970030914 ◽

1997 ◽

Vol 3 (9) ◽

pp. 1472-1481 ◽

Author(s):

Shū Kobayashi ◽

Mineko Horibe

Keyword(s):

Lewis Acids ◽

Aldol Reactions ◽

Controlled Synthesis ◽

Asymmetric Aldol ◽

Chiral Lewis Acid ◽

Chiral Diamines

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Synthesis, Resolution, and Aldol Reactions of a Planar-Chiral Lewis Acid Complex.

10.1002/chin.200612030 ◽

2006 ◽

Vol 37 (12) ◽

Author(s):

Shih-Yuan Liu ◽

Ivory D. Hills ◽

Gregory C. Fu

Keyword(s):

Aldol Reactions ◽

Acid Complex ◽

Chiral Lewis Acid

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ChemInform Abstract: A Novel Chiral Zirconium Catalyst for Enantioselective Aldol and Mannich-Type Reactions. Catalytic Activation of Both Aldehydes and Imines Using a Similar Chiral Lewis Acid.

10.1002/chin.200120032 ◽

2001 ◽

Vol 32 (20) ◽

pp. no-no

Author(s):

Shu Kobayashi ◽

Haruro Ishitani ◽

Yasuhiro Yamashita ◽

Masaharu Ueno ◽

Haruka Shimizu

Keyword(s):

Catalytic Activation ◽

Chiral Lewis Acid

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Enantioselective conjugate radical addition reactions mediated by chiral Lewis acid complexes of (R,R)-4,6-dibenzofurandiyl-2,2′-bis(4-phenyloxazoline) (DBFOX/Ph)

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(99)00238-4 ◽

1999 ◽

Vol 10 (12) ◽

pp. 2417-2428 ◽

Author(s):

Ulrich Iserloh ◽

Dennis P Curran ◽

Shuji Kanemasa

Keyword(s):

Radical Addition ◽

Addition Reactions ◽

Chiral Lewis Acid

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Enantioselective 2-Alkylation of 3-Substituted Indoles with Dual Chiral Lewis Acid/Hydrogen-Bond-Mediated Catalyst

Organic Letters ◽

10.1021/acs.orglett.6b03500 ◽

2016 ◽

Vol 19 (1) ◽

pp. 222-225 ◽

Author(s):

Zijun Zhou ◽

Yanjun Li ◽

Lei Gong ◽

Eric Meggers

Keyword(s):

Hydrogen Bond ◽

Chiral Lewis Acid

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Nickel(ii)-catalyzed enantioselective cyclopropanation of 3-alkenyl-oxindoles with phenyliodonium ylide via free carbene

Chemical Science ◽

10.1039/c5sc03658e ◽

2016 ◽

Vol 7 (4) ◽

pp. 2717-2721 ◽

Author(s):

Jing Guo ◽

Yangbin Liu ◽

Xiangqiang Li ◽

Xiaohua Liu ◽

Lili Lin ◽

...

Keyword(s):

Epr Spectroscopy ◽

Spectroscopy Study ◽

Chiral Lewis Acid

A chiral Lewis acid-promoted cyclopropanation using a phenyliodonium ylide as the carbene precursor was developed. An EPR spectroscopy study supported a stepwise biradical mechanism.

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