Bond fixation in annulenes. 9. Equalization of ring inversion and bond shifting energetics in 1,2,3,4-tetramethylcyclooctatetraene. Asymmetric synthesis direct resolution, and absolute configuration of the optically active hydrocarbon

Leo A. Paquette; John M. Gardlik; Larry K. Johnson; Kevin J. McCullough

doi:10.1021/ja00535a033

Bond fixation in annulenes. 9. Equalization of ring inversion and bond shifting energetics in 1,2,3,4-tetramethylcyclooctatetraene. Asymmetric synthesis direct resolution, and absolute configuration of the optically active hydrocarbon

Journal of the American Chemical Society ◽

10.1021/ja00535a033 ◽

1980 ◽

Vol 102 (15) ◽

pp. 5026-5032 ◽

Cited By ~ 20

Author(s):

Leo A. Paquette ◽

John M. Gardlik ◽

Larry K. Johnson ◽

Kevin J. McCullough

Keyword(s):

Asymmetric Synthesis ◽

Absolute Configuration ◽

Optically Active ◽

Ring Inversion

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ChemInform Abstract: BOND FIXATION IN ANNULENES. 9. EQUALIZATION OF RING INVERSION AND BOND SHIFTING ENERGETICS IN 1,2,3,4-TETRAMETHYLCYCLOOCTATETRAENE. ASYMMETRIC SYNTHESIS DIRECT RESOLUTION, AND ABSOLUTE CONFIGURATION OF THE OPTICALLY ACTIVE HYDROCARBON

Chemischer Informationsdienst ◽

10.1002/chin.198043144 ◽

1980 ◽

Vol 11 (43) ◽

Author(s):

L. A. PAQUETTE ◽

J. M. GARDLIK ◽

L. K. JOHNSON ◽

K. J. MCCULLOUGH

Keyword(s):

Asymmetric Synthesis ◽

Absolute Configuration ◽

Optically Active ◽

Ring Inversion

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A GENERAL METHOD FOR ESTABLISHING THE ABSOLUTE CONFIGURATION OF OPTICALLY ACTIVE BIPHENYLS BY ASYMMETRIC SYNTHESIS

Journal of the American Chemical Society ◽

10.1021/ja01564a072 ◽

1957 ◽

Vol 79 (7) ◽

pp. 1769-1769 ◽

Cited By ~ 4

Author(s):

Kurt Mislow ◽

Paul Newman

Keyword(s):

Asymmetric Synthesis ◽

Absolute Configuration ◽

Optically Active ◽

The Absolute ◽

General Method

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ChemInform Abstract: STEREOCHEMICAL STUDIES PART 24, ASYMMETRIC SYNTHESIS OF OPTICALLY ACTIVE (+)-4-METHYL-4-PHENYL-2-CYCLOHEXENONE WITH ENAMINE ALKYLATION USING PROLINE DERIVATIVES PART 25, THE ABSOLUTE CONFIGURATION AND OPTICAL PURITY OF (+)-4-METHYL-4-

Chemischer Informationsdienst ◽

10.1002/chin.197405222 ◽

1974 ◽

Vol 5 (5) ◽

pp. no-no

Author(s):

G. OTANI ◽

Y. YAMADA

Keyword(s):

Asymmetric Synthesis ◽

Absolute Configuration ◽

Optical Purity ◽

Optically Active ◽

The Absolute ◽

Proline Derivatives

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ChemInform Abstract: Prediction of the Absolute Configuration of Optically Active Pheromones Using Liquid Crystals

ChemInform ◽

10.1002/chin.199331274 ◽

2010 ◽

Vol 24 (31) ◽

pp. no-no

Author(s):

T. IKEMOTO ◽

K. MITSUHASHI ◽

K. MORI

Keyword(s):

Liquid Crystals ◽

Absolute Configuration ◽

Optically Active ◽

The Absolute

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Asymmetric synthesis of aerothionin, a marine dimeric spiroisoxazoline natural product, employing optically active spiroisoxazoline derivative

Tetrahedron Letters ◽

10.1016/j.tetlet.2005.11.097 ◽

2006 ◽

Vol 47 (5) ◽

pp. 727-731 ◽

Cited By ~ 30

Author(s):

Takahisa Ogamino ◽

Rika Obata ◽

Shigeru Nishiyama

Keyword(s):

Asymmetric Synthesis ◽

Natural Product ◽

Optically Active

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Central–axial–central chirality transfer: asymmetric synthesis of highly substituted indenes bearing a stereogenic quaternary carbon center from optically active propargyl alcohols

Chemical Communications ◽

10.1039/c4cc08034c ◽

2015 ◽

Vol 51 (2) ◽

pp. 380-383 ◽

Cited By ~ 27

Author(s):

Masahiro Egi ◽

Kaori Shimizu ◽

Marin Kamiya ◽

Yuya Ota ◽

Shuji Akai

Keyword(s):

Asymmetric Synthesis ◽

Optically Active ◽

Quaternary Carbon ◽

Chirality Transfer ◽

Propargyl Alcohols

An asymmetric synthesis of highly substituted indenes has been developed via the central–axial–central chirality transfer from optically active propargyl alcohols.

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Asymmetric Synthesis ofα-Methylα-Amino Acids by Diastereoselective Alkylation of Optically Active 6-Isopropyl-3-methyl-2,3—dihydro-6H-1,4-oxazin-2-ones

Angewandte Chemie International Edition in English ◽

10.1002/anie.199709951 ◽

1997 ◽

Vol 36 (9) ◽

pp. 995-997 ◽

Cited By ~ 35

Author(s):

Rafael Chinchilla ◽

Larry R. Falvello ◽

Nuria Galindo ◽

Carmen Nájera

Keyword(s):

Amino Acids ◽

Asymmetric Synthesis ◽

Optically Active

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ChemInform Abstract: Asymmetric Synthesis of Optically Active Alcohols with Two Chiral Centres from a Racemic Aldehyde by the Selective Addition of Dialkylzinc Reagents Using Chiral Catalysts.

ChemInform ◽

10.1002/chin.199147046 ◽

2010 ◽

Vol 22 (47) ◽

pp. no-no

Author(s):

S. NIWA ◽

T. HATANAKA ◽

K. SOAI

Keyword(s):

Asymmetric Synthesis ◽

Optically Active ◽

Chiral Catalysts ◽

Selective Addition

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ChemInform Abstract: Preparation of Optically Active Secondary Amines by Thermal Decomposition of (Methylbenzyl)urea Analogs: Absolute Configuration of (+)- and (-)-Mecamylamine.

Chemischer Informationsdienst ◽

10.1002/chin.198624331 ◽

1986 ◽

Vol 17 (24) ◽

Author(s):

B. SCHOENENBERGER ◽

A. BROSSI ◽

C. GEORGE ◽

J. L. FLIPPEN-ANDERSON

Keyword(s):

Thermal Decomposition ◽

Absolute Configuration ◽

Optically Active ◽

Secondary Amines

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Optically Active Triptycenes. VII. Synthesis, Optical Resolution and Absolute Configuration of 3-Chloro and 4-Chloro-7-substituted Triptycenes.

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.47.1761 ◽

1974 ◽

Vol 47 (7) ◽

pp. 1761-1766 ◽

Cited By ~ 5

Author(s):

Michiaki Hashimoto ◽

Yasumi Shimizu ◽

Fumio Ogura ◽

Masazumi Nakagawa

Keyword(s):

Absolute Configuration ◽

Optical Resolution ◽

Optically Active

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