Absolute stereochemistries of -2,3-disubstituted spirocyclopropane-1,9′-fluorene derivatives: A styryl modification cd-method for carboxyl substituted chiral centers-Reference-Cited by-同舟云学术

Absolute stereochemistries of -2,3-disubstituted spirocyclopropane-1,9′-fluorene derivatives: A styryl modification cd-method for carboxyl substituted chiral centers

Published:1986-01 Issue:37 Volume:27 Page:4493-4496
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Okada Keiji,Samizo Fumio,Oda Masaji,Harada Nobuyuki,Uda Hisashi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. K. Okada, F. Samizo and M. Oda, J. Chem. Soc., Chem. Commun, in press.

2. Exciton chirality method and its application to configurational and conformational studies of natural products

3. Structure of the dimethyl sulfoxide-oxalyl chloride reaction product. Oxidation of heteroaromatic and diverse alcohols to carbonyl compounds

4. The absorption and circular dichroism spectra and the absolute configuration of (+)-1-fluoro-12-methylbenzo[c] phenanthrene

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3. Photoisomerization Studied by Stepwise Two-Color Two-Photon Excitation. 2. .alpha.-(10''-Cyanoanthracen-9''-yl)ethyl Spiro[cyclopropane-1,9'-fluorene]-2-carboxylates;The Journal of Physical Chemistry;1995-03

4. Asymmetric induction via intramolecular T2-sensitization: Photoisomerization of α-(9″-anthryl)ethyl spiro[cyclopropane-1,9′-fluorene]-2-carboxylates;Tetrahedron Letters;1989-01

5. Stereocontrol by energy transfer: photoisomerization of .alpha.-arylalkyl spiro[cyclopropane-1,9'-fluorene]-2-carboxylate;Journal of the American Chemical Society;1987-09