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Chiral, triformylphenol-derived salen-type [4 + 6] organic cages

Organic & biomolecular chemistry, 2016-01, Vol.14 (31), p.7495-7499

2016

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Designing Large Triangular Chiral Macrocycles: Efficient [3 + 3] Diamine−Dialdehyde Condensations Based on Conformational Bias

Journal of organic chemistry, 2000-09, Vol.65 (18), p.5768-5773

2000

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Chiral calixsalen-type macrocycles from trans-1,2-diaminocyclohexane

Tetrahedron: asymmetry, 2003-05, Vol.14 (10), p.1303-1308

2003

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Fine tuning of molecular and supramolecular properties of simple trianglimines – the role of the functional group

RSC advances, 2016, Vol.6 (58), p.53358-53369

2016

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Helicity of N, N′-diaryl- trans-1,2-diaminocyclohexane derivatives. Implications for molecular helicity manipulations

Tetrahedron, 2003-11, Vol.59 (47), p.9323-9331

2003

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Convenient Enantioselective Hydrosilylation of Ketones Catalyzed by Zinc‐Macrocyclic Oligoamine Complexes

Advanced synthesis & catalysis, 2009-05, Vol.351 (7‐8), p.1055-1063

2009

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Chiral, triformylphenol-derived salen-type [4 + 6] organic cagesDedicated to Prof. Bogdan Marciniec on the occasion of his 75 birthday.Electronic supplementary information (ESI) available: Experimental procedures, calculation details, copies of NMR, MS and IR spectra, Fig. SI_1-SI_38, X-ray, PXRD and TGA data, full Gaussian citation, and tabulated total and relative energies for calculated structures and Cartesian coordinates. CCDC 1477553. For ESI and crystallographic data in CIF or other elect

2016-08

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Trianglamines-Readily Prepared, Conformationally Flexible Inclusion-Forming Chiral Hexamines

Chemistry : a European journal, 2006-02, Vol.12 (6), p.1807-1817

2006

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Fine tuning of molecular and supramolecular properties of simple trianglimines - the role of the functional groupDedicated to Prof. Janusz Jurczak on the occasion of his 75 birthday.Electronic supplementary information (ESI) available: Experimental procedures, calculation details, copies of NMR, MS and IR spectra, Fig. SI_1-SI_55, tabulated total and relative energies for calculated structures, Cartesian coordinates, conditions and retention times for HPLC separation of enantiomers, literature r

2016-06

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RhombiminesCyclic Tetraimines of trans-1,2-Diaminocyclohexane Shaped by the Diaryl Ether Structural Motif

Journal of organic chemistry, 2005-11, Vol.70 (24), p.10147-10150

2005

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Helicity Induction in a Bichromophore: A Sensitive and Practical Chiroptical Method for Absolute Configuration Determination of Aliphatic Alcohols

Organic letters, 2002-11, Vol.4 (24), p.4185-4188

2002

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Absolute Configuration, Conformation, and Circular Dichroism of Monocyclic Arene Dihydrodiol Metabolites: It is All Due to the Heteroatom Substituents

Journal of the American Chemical Society, 2005-03, Vol.127 (12), p.4308-4319

2005

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Synthesis, structure, and contrasting chiroptical properties of large trianglimine macrocycles

Chirality (New York, N.Y.), 2005, Vol.17 (S1), p.S93-S100

2005

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A circular dichroism detection of stereostructural change due to amine protonation

Tetrahedron letters, 2003-11, Vol.44 (45), p.8311-8314

2003

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Circular Dichroism of 9,10-Dihydrophenanthrene Derivatives Reveals both the Absolute Configuration and Conformation: A Novel Approach to Mislow's Helicity Rule

Chemistry : a European journal, 2002-09, Vol.8 (18), p.4210-4215

2002

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Induced homohelicity of diphenimide bis-propellers

New journal of chemistry, 2002, Vol.26 (12), p.1714-1717

2002

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Structure and unexpected chiroptical properties of chiral 4-pyrrolidinyl substituted 2(5H)-furanones

Chirality (New York, N.Y.), 2004, Vol.16 (7), p.405-413

2004

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Induction of chirality in donor–acceptor spiro compounds

Mendeleev communications, 2003, Vol.13 (3), p.139-140

2003

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Contrasting chiroptical properties of sparteine lactams and thiolactams

Tetrahedron: asymmetry, 2001-06, Vol.12 (9), p.1337-1343

2001

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Energy Conservation: A New Force Has Entered the Scene: The Residential End-user, and "Sophisticated Convenience"

Strategic planning for energy and the environment, 2001-01, Vol.20 (3), p.31-49

2001

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3.11 - Trianglamines and Related Chiral Macrocycles

Comprehensive Supramolecular Chemistry II, 2017, p.267-291

Second Edition, 2017

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Needed: Electric Submetering: "MASTER-METERING" IN COOPERATIVE HOUSING IS UNFAIR, EXPENSIVE, WASTES ENERGY

Strategic planning for energy and the environment, 1997-01, Vol.16 (3), p.68-78

1997

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Designing large triangular chiral macrocycles: efficient

Journal of organic chemistry, 2000-09, Vol.65 (18), p.5768-5773

2000

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Part Two of the Series on Energy Conservation

Strategic planning for energy and the environment, 2001-01, Vol.20 (3), p.31-49

2001

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ENERGY CONSERVATION Energy Efficiency, the Environment, and A New Role for the End-User

Strategic planning for energy and the environment, 2000-10, Vol.20 (2), p.6-25

2000

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Chiral, triformylphenol-derived salen-type [4 + 6] organic cages

Designing Large Triangular Chiral Macrocycles: Efficient [3 + 3] Diamine−Dialdehyde Condensations Based on Conformational Bias

Chiral calixsalen-type macrocycles from trans-1,2-diaminocyclohexane

Fine tuning of molecular and supramolecular properties of simple trianglimines – the role of the functional group

Helicity of N, N′-diaryl- trans-1,2-diaminocyclohexane derivatives. Implications for molecular helicity manipulations

Convenient Enantioselective Hydrosilylation of Ketones Catalyzed by Zinc‐Macrocyclic Oligoamine Complexes

Trianglamines-Readily Prepared, Conformationally Flexible Inclusion-Forming Chiral Hexamines

RhombiminesCyclic Tetraimines of trans-1,2-Diaminocyclohexane Shaped by the Diaryl Ether Structural Motif

Helicity Induction in a Bichromophore: A Sensitive and Practical Chiroptical Method for Absolute Configuration Determination of Aliphatic Alcohols

Absolute Configuration, Conformation, and Circular Dichroism of Monocyclic Arene Dihydrodiol Metabolites: It is All Due to the Heteroatom Substituents

Synthesis, structure, and contrasting chiroptical properties of large trianglimine macrocycles

A circular dichroism detection of stereostructural change due to amine protonation

Circular Dichroism of 9,10-Dihydrophenanthrene Derivatives Reveals both the Absolute Configuration and Conformation: A Novel Approach to Mislow's Helicity Rule

Induced homohelicity of diphenimide bis-propellers

Structure and unexpected chiroptical properties of chiral 4-pyrrolidinyl substituted 2(5H)-furanones

Induction of chirality in donor–acceptor spiro compounds

Contrasting chiroptical properties of sparteine lactams and thiolactams

Energy Conservation: A New Force Has Entered the Scene: The Residential End-user, and "Sophisticated Convenience"

3.11 - Trianglamines and Related Chiral Macrocycles

Needed: Electric Submetering: "MASTER-METERING" IN COOPERATIVE HOUSING IS UNFAIR, EXPENSIVE, WASTES ENERGY

Designing large triangular chiral macrocycles: efficient

Part Two of the Series on Energy Conservation

ENERGY CONSERVATION Energy Efficiency, the Environment, and A New Role for the End-User

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