ChemInform Abstract: Assignment of the Absolute Configuration to Winterstein′s Acid, (R)-3-Dimethylamino-3-phenyl Propionic Acid, by the Asymmetric Synthesis of Homochiral (S)-(+)-Ethyl 3-Dimethylamino-3-phenyl Propionate.

S. G. DAVIES; J. DUPONT; R. J. C. EASTON

doi:10.1002/chin.199040294

ChemInform Abstract: Assignment of the Absolute Configuration to Winterstein′s Acid, (R)-3-Dimethylamino-3-phenyl Propionic Acid, by the Asymmetric Synthesis of Homochiral (S)-(+)-Ethyl 3-Dimethylamino-3-phenyl Propionate.

ChemInform ◽

10.1002/chin.199040294 ◽

1990 ◽

Vol 21 (40) ◽

Author(s):

S. G. DAVIES ◽

J. DUPONT ◽

R. J. C. EASTON

Keyword(s):

Asymmetric Synthesis ◽

Propionic Acid ◽

Absolute Configuration ◽

Phenyl Propionic Acid ◽

The Absolute

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Assignment of the absolute configuration to winterstein's acid, R-3-dimethylamino-3-phenyl propionic acid, by the asymmetric synthesis of homochiral (S)-(+)-ethyl 3-dimetylamino-3-phenyl propionate

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)86312-0 ◽

1990 ◽

Vol 1 (5) ◽

pp. 279-280 ◽

Cited By ~ 17

Author(s):

Stephen G. Davies ◽

Jairton Dupont ◽

Robert J.C. Easton

Keyword(s):

Asymmetric Synthesis ◽

Propionic Acid ◽

Absolute Configuration ◽

Phenyl Propionic Acid ◽

The Absolute

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A Facile Route to alpha-Hydrazinopropionic Acid of High Optical Purity. The Absolute Configuration of alpha-(4,5,6,7-Tetrahydroindazolyl-1- and -2)propionic Acid.

Acta Chemica Scandinavica ◽

10.3891/acta.chem.scand.29b-0093 ◽

1975 ◽

Vol 29b ◽

pp. 93-98 ◽

Cited By ~ 10

Author(s):

Håkan Gustafsson ◽

Carmen H. G. Vogt ◽

Curt R. Enzell ◽

O. Smidsrød ◽

O. Dahl ◽

...

Keyword(s):

Propionic Acid ◽

Absolute Configuration ◽

Optical Purity ◽

High Optical Purity ◽

The Absolute ◽

Hydrazinopropionic Acid ◽

Facile Route

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ChemInform Abstract: Asymmetric Synthesis of 5,5-Disubstituted Thiotetronic Acids Using an Allyl Xanthate to Dithiocarbonate Rearrangement: Total Synthesis of ( 5S)-Thiolactomycin with Revision of the Absolute Configuration of the Natural Product.

ChemInform ◽

10.1002/chin.199729101 ◽

2010 ◽

Vol 28 (29) ◽

pp. no-no

Author(s):

M. S. CHAMBERS ◽

E. J. THOMAS

Keyword(s):

Total Synthesis ◽

Asymmetric Synthesis ◽

Natural Product ◽

Absolute Configuration ◽

The Absolute

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Asymmetric syntheses. Part VIII. Asymmetric synthesis of β-allenic alcohols with the lithium aluminium hydride–3-O-benzyl-1,2-O-cyclohexylidene-α-D-glucofuranose complex; determination of the absolute configuration of marasin (nona-3,4-diene-6,8-diyn-1-ol) and 9-methylmarasin (deca-3,4-diene-6,8-diyn-1-ol)

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19740000557 ◽

1974 ◽

pp. 557-561 ◽

Cited By ~ 8

Author(s):

Stephen R. Landor ◽

Brian J. Miller ◽

John P. Regan ◽

Austin R. Tatchell

Keyword(s):

Asymmetric Synthesis ◽

Absolute Configuration ◽

Lithium Aluminium Hydride ◽

Asymmetric Syntheses ◽

Lithium Aluminium ◽

The Absolute

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Total synthesis of (W) maculalactone A, maculalactone B and maculalactone C and the determination of the absolute configuration of natural (+) maculalactone A by asymmetric synthesis

Tetrahedron ◽

10.1016/s0040-4020(04)00621-0 ◽

2004 ◽

Author(s):

G BROWN

Keyword(s):

Total Synthesis ◽

Asymmetric Synthesis ◽

Absolute Configuration ◽

The Absolute

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ChemInform Abstract: Asymmetric Synthesis and Determination of the Absolute Configuration of FK584, an Agent for the Treatment of Overactive Detrusor.

ChemInform ◽

10.1002/chin.200120078 ◽

2001 ◽

Vol 32 (20) ◽

pp. no-no

Author(s):

Kazuhiko Take ◽

Kazuo Okumura ◽

Kazunori Tsubaki ◽

Kiyoshi Taniguchi ◽

Youichi Shiokawa

Keyword(s):

Asymmetric Synthesis ◽

Absolute Configuration ◽

Overactive Detrusor ◽

The Absolute

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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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Central to axial chirality transfer via double bond migration: asymmetric synthesis and determination of the absolute configuration of axially chiral 1-(3′-indenyl)naphthalenes

Chemical Communications ◽

10.1039/cc9960002571 ◽

1996 ◽

pp. 2571-2572 ◽

Cited By ~ 23

Author(s):

Robert W. Baker ◽

Trevor W. Hambley ◽

Peter Turner ◽

Brian J. Wallace

Keyword(s):

Double Bond ◽

Asymmetric Synthesis ◽

Absolute Configuration ◽

Chirality Transfer ◽

Double Bond Migration ◽

Axial Chirality ◽

Axially Chiral ◽

The Absolute

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Determination of absolute configuration of the derivative from 2-[4-(1-oxo-2-isoindolinyl)-phenyl]-propionic acid and R-(+)-1-phenylethylamine by 1H-NMR spectroscopy; use of shift reagent with diastereoisomeric amides

Tetrahedron Letters ◽

10.1016/0040-4039(80)80022-0 ◽

1980 ◽

Vol 21 (23) ◽

pp. 2273-2276 ◽

Cited By ~ 11

Author(s):

Sergio De Munari ◽

Giuseppe Marazzi ◽

Angelo Forgione ◽

Antonio Longo ◽

Paolo Lombardi

Keyword(s):

Nmr Spectroscopy ◽

Propionic Acid ◽

1H Nmr ◽

Absolute Configuration ◽

1H Nmr Spectroscopy ◽

Shift Reagent ◽

Phenyl Propionic Acid ◽

Determination Of Absolute Configuration

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Asymmetric synthesis of β-hydroxyesters by aldol type condensation of enantiomerically pure t -butyl p -tolyl sulfinyl acetate: unexpected substituent effect on the absolute configuration of the product

Tetrahedron Letters ◽

10.1016/s0040-4039(01)00318-5 ◽

2001 ◽

Vol 42 (15) ◽

pp. 2923-2925 ◽

Cited By ~ 6

Author(s):

Guy Solladié ◽

Claude Bauder ◽

Eva Arce-Dubois ◽

Yacine Pasturel-Jacopé

Keyword(s):

Asymmetric Synthesis ◽

Absolute Configuration ◽

Substituent Effect ◽

Enantiomerically Pure ◽

The Absolute

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