ChemInform Abstract: Central to Axial Chirality Transfer via Double Bond Migration: Asymmetric Synthesis and Determination of the Absolute Configuration of Axially Chiral 1-(3′-Indenyl)naphthalenes

R. W. BAKER; T. W. HAMBLEY; P. TURNER; B. J. WALLACE

doi:10.1002/chin.199713073

ChemInform Abstract: Central to Axial Chirality Transfer via Double Bond Migration: Asymmetric Synthesis and Determination of the Absolute Configuration of Axially Chiral 1-(3′-Indenyl)naphthalenes

ChemInform ◽

10.1002/chin.199713073 ◽

2010 ◽

Vol 28 (13) ◽

pp. no-no

Author(s):

R. W. BAKER ◽

T. W. HAMBLEY ◽

P. TURNER ◽

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

Tetrahedron ◽

10.1016/j.tet.2004.04.060 ◽

2004 ◽

Vol 60 (25) ◽

pp. 5439-5451 ◽

Cited By ~ 24

Author(s):

Geoffrey D Brown ◽

Ho-Fai Wong

Keyword(s):

Total Synthesis ◽

Asymmetric Synthesis ◽

Absolute Configuration ◽

The Absolute

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Total Synthesis of (.+-.)-Maculalactone A (rac-(I)), Maculalactone B (II) and Maculalactone C (III) and the Determination of the Absolute Configuration of Natural (+)-Maculalactone A by Asymmetric Synthesis.

ChemInform ◽

10.1002/chin.200440214 ◽

2004 ◽

Vol 35 (40) ◽

Author(s):

Geoffrey D. Brown ◽

Ho-Fai Wong

Keyword(s):

Total Synthesis ◽

Asymmetric Synthesis ◽

Absolute Configuration ◽

The Absolute

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Central-to-axial chirality transfer revealed by liquid crystals: A combined experimental and computational approach for the determination of absolute configuration of carboxylic acids with an α chirality centre

Chirality ◽

10.1002/chir.20969 ◽

2011 ◽

Vol 23 (9) ◽

pp. 736-743 ◽

Cited By ~ 2

Author(s):

Alberta Ferrarini ◽

Fiammetta Ferroni ◽

Silvia Pieraccini ◽

Carlo Rosini ◽

Stefano Superchi ◽

...

Keyword(s):

Liquid Crystals ◽

Carboxylic Acids ◽

Absolute Configuration ◽

Computational Approach ◽

Chirality Transfer ◽

Axial Chirality ◽

Determination Of Absolute Configuration

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Determination of the Absolute Configuration of CN-Palladacycles by 31P{1H} NMR Spectroscopy Using (1R,2S,5R)-Menthyloxydiphenylphosphine as the Chiral Derivatizing Agent: Efficient Chirality Transfer in Phosphinite Adducts

Organometallics ◽

10.1021/acs.organomet.5b00706 ◽

2016 ◽

Vol 35 (2) ◽

pp. 75-90 ◽

Cited By ~ 6

Author(s):

Olga N. Gorunova ◽

Ivan M. Novitskiy ◽

Yuri K. Grishin ◽

Igor P. Gloriozov ◽

Vitaly A. Roznyatovsky ◽

...

Keyword(s):

Nmr Spectroscopy ◽

1H Nmr ◽

Absolute Configuration ◽

1H Nmr Spectroscopy ◽

Chirality Transfer ◽

Derivatizing Agent ◽

Chiral Derivatizing Agent ◽

The Absolute

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Determination of the absolute configuration of vibsanin F by asymmetric synthesis via π-allylpalladium complex

Tetrahedron Letters ◽

10.1016/s0040-4039(03)01537-5 ◽

2003 ◽

Vol 44 (33) ◽

pp. 6235-6239 ◽

Cited By ~ 16

Author(s):

Hiroaki Yuasa ◽

Gouki Makado ◽

Yoshiyasu Fukuyama

Keyword(s):

Asymmetric Synthesis ◽

Absolute Configuration ◽

The Absolute

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

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.48.1903 ◽

2000 ◽

Vol 48 (12) ◽

pp. 1903-1907 ◽

Cited By ~ 4

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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