Stereoselective bidirectional synthesis of spiroacetals via Rh(II)-catalysed double C

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Stereoselective bidirectional synthesis of spiroacetals via Rh(II)-catalysed double C–H insertion

Published:2018-03 Issue:12 Volume:74 Page:1313-1321
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Lepage Romain J.,Coster Mark J.

Funder

Griffith University

Memorial Sloan-Kettering Cancer Center

Australian Research Council's

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference44 articles.

1. Chemistry of spiroketals

2. Chemistry of fruit flies

3. Spiroacetals in Insects

4. Biosynthesis of insect spiroacetals

5. 2-Ethyl-1,6-dioxaspiro[4.4]nonane, principal aggregation pheromone of Pityogenes chalcographus (L.)

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1. The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2018;Coordination Chemistry Reviews;2019-12

2. Tandem Achmatowicz Rearrangement and Acetalization of 1-[5-(Hydroxyalkyl)-furan-2-yl]-cyclobutanols Leading to Dispiroacetals and Subsequent Ring-Expansion to Form 6,7-Dihydrobenzofuran-4(5H)-ones;The Journal of Organic Chemistry;2018-09-21

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