Gold-catalyzed diastereoselective synthesis of 2,6-trans-disubstituted tetrahydropyran derivatives: application for the synthesis of the C1–C13 fragment of bistramide A and B-Reference-Cited by-同舟云学术

Gold-catalyzed diastereoselective synthesis of 2,6-trans-disubstituted tetrahydropyran derivatives: application for the synthesis of the C1–C13 fragment of bistramide A and B

Published:2015 Issue:117 Volume:5 Page:96758-96768
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Padhi Birakishore¹²³⁴⁵,Reddy D. Srinivas¹²³⁴,Mohapatra Debendra K.¹²³⁴⁵

Affiliation:

1. Natural Products Chemistry Division

2. CSIR-Indian Institute of Chemical Technology

3. Hyderabad-500007

4. India

5. Academy of Scientific and Innovative Research

Abstract

An efficient Au(iii)-catalyzed diastereoselective allylation leading to 2,6-trans-disubstituted tetrahydropyrans and application for the synthesis of the C1–C13 fragment of bistramide A and B is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA17646H

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3. Bismuth bromide as an efficient and versatile catalyst for the cyanation and allylation of carbonyl compounds and acetals with organosilicon reagents

4. Rhenium complex-catalyzed allylation of acetals with allyltrimethylsilane

5. Strategies for the construction of tetrahydropyran rings in the synthesis of natural products

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