Highly-functionalised difluorinated cyclohexane polyols via the Diels–Alder reaction: regiochemical control via the phenylsulfonyl group-Reference-Cited by-同舟云学术

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Highly-functionalised difluorinated cyclohexane polyols via the Diels–Alder reaction: regiochemical control via the phenylsulfonyl group

Published:2005 Issue:18 Volume:3 Page:3297
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Crowley Patrick J.,Fawcett John,Griffith Gerry A.,Moralee Andrew C.,Percy Jonathan M.,Salafia Vittoria

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2005/OB/B507131C

Reference90 articles.

1. Derivatives of 7-oxabicyclo[2.2.1]heptane in nature and as useful synthetic intermediates

2. Chemistry of Inositol Lipid Mediated Cellular Signaling

3. Cyclitols: Conduritols and Related Compounds

4. The first enantiocontrolled synthesis of naturally occurring polyoxygenated cyclohexenylmethanol dibenzoates (–)-zeylenol, (–)-uvarigranol G, (–)-tonkinenin A and (+)-pipoxide

5. Synthesis of a protected derivative of (±)-1-(hydroxymethyl)conduritol C from 2-(hydroxymethyl)furan

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3. 8.28 Reduction of SulfurCarbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon;Comprehensive Organic Synthesis II;2014

4. Synthesis of 7-Oxabicyclo[2.2.1]heptane and Derivatives;Synthesis of Saturated Oxygenated Heterocycles I;2013-12-10

5. Fluoro-C-glycosides and fluoro-carbasugars, hydrolytically stable and synthetically challenging glycomimetics;Chem. Soc. Rev.;2013

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