Conformational preferences of oxy-substituents in butenolide–tetrahydropyran spiroacetals and butenolide–piperidine spiro-N,O-acetals-Reference-Cited by-同舟云学术

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Conformational preferences of oxy-substituents in butenolide–tetrahydropyran spiroacetals and butenolide–piperidine spiro-N,O-acetals

Published:2012 Issue:17 Volume:10 Page:3506
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Naud Sébastien,Macnaughton Sarah J.,Dyson Bryony S.,Woollaston Daniel J.,Dallimore Jonathan W. P.,Robertson Jeremy

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2012/OB/C2OB06849D

Reference47 articles.

1. The synthesis of 7-methyl-1,6-dioxa-2-spiro[4,4]nonanacetic (i.e. exogonic) acid

2. A Convenient Method for the Formation of 2-Oxo-1,6-dioxaspiroalkene Rings

3. A photo-oxidative analogue of the clauson-kaas reaction

4. A general approach to the stereoselective synthesis of spiroketals. A total synthesis of the pheromones of the olive fruit fly and related compounds

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