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Journal ArticleDOI

Reaction of Resorcinol With Acetone.

Peter Livant, +2 more
- 07 Feb 1997 - 
- Vol. 62, Iss: 3, pp 737-742
About
This article is published in Journal of Organic Chemistry.The article was published on 1997-02-07. It has received 24 citations till now. The article focuses on the topics: Resorcinol & Acetone.

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Citations
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Biobased thermosetting epoxy: present and future.

TL;DR: This paper aims to provide a history of the use of glass in the construction of buildings in Montpellier and its applications in the 21st Century.
Journal ArticleDOI

A facile strategy to achieve fully bio-based epoxy thermosets from eugenol

TL;DR: In this paper, the authors proposed a facile strategy to achieve epoxy thermosets with 100% bio-based content, which includes the preparation of four bio-bio-based epoxy resins and their thermoset through the self-curing reaction of 1-4.
Journal ArticleDOI

Biobased phenol and furan derivative coupling for the synthesis of functional monomers

TL;DR: In this article, an overview of the different synthetic methods to prepare aromatic building blocks via various coupling methods is presented, focusing on the synthesis of C-C bonds, reductive coupling of natural aldehydes, carbonyl-aromatic coupling and other various routes to prepare monomers.
Journal ArticleDOI

Synthesis and Properties of Spiro-Centered Benzoxazines

TL;DR: A series of thermally stable spiro-centered bis(benzoxazine) monomers (BPSPI/SPBC-Bz)s was synthesized using spirobiindane/spirobischroman phenol, different amines (aniline, p-toluidine, and 2-(4-aminophenyl)ethanol) and paraformaldehyde and was characterized by FT-IR, 1H and 13C NMR, and elemental analysis as discussed by the authors.
Journal ArticleDOI

Visual Sensing of Saccharides Promoted by Resorcinol Condensation Products

TL;DR: Heating aqueous DMSO solutions of five saccharides in the presence of 1-3 reveals that each receptor promotes solution colors characteristic for each sugar.
References
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Book

Stereochemistry of Organic Compounds

TL;DR: Stereochemistry of Alkenes Conformation of Acyclic Molecules Configuration and conformation of cyclic Molecule Stereoselective Synthesis Chiroptical Properties Chirality in Molecules Devoid of Chiral Centres as discussed by the authors.
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A comparison of conformational energies calculated by molecular mechanics (MM2(85),#Sybyl 5.1,#Sybyl 5.21, and ChemX) and semiempirical (AM1 and PM3) methods

TL;DR: In this article, the conformational energies of different conformers have been calculated for a series of molecules using various molecular mechanics and semi-empirical methods, and the quality of the force fields has also been tested by calculating barriers to rotation about carbon-carbon bonds.