Denovo asymmetric synthesis of the mezzettiaside family of natural products via the iterative use of a dual B-/Pd-catalyzed glycosylation-Reference-Cited by-同舟云学术

Denovo asymmetric synthesis of the mezzettiaside family of natural products via the iterative use of a dual B-/Pd-catalyzed glycosylation

Published:2014 Issue:6 Volume:5 Page:2230-2234
ISSN:2041-6520
Container-title:Chem. Sci.
language:en
Short-container-title:Chem. Sci.

Author:

Bajaj Sumit O.¹²³,Sharif Ehesan U.¹²³,Akhmedov Novruz G.⁴⁵⁶,O'Doherty George A.¹²³

Affiliation:

1. Department of Chemistry and Chemical Biology

2. Northeastern University

3. Boston, USA

4. Department of Chemistry

5. West Virginia University

6. Morgantown, USA

Abstract

Synthesis of the mezzettiaside family of natural products via the iterative use of a dual nucleophilic boron/electrophilic Pd-catalyzed glycosylation.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/SC/C4SC00593G

Reference37 articles.

1. Chemistry of the annonaceae, Part 29. Structure of mezzettiaside-2, -4, -5, -6 and -7, new partially esterified 1-O-octyl tri- and tetra-rhamnosyl derivatives from Mezzettia leptopoda

2. Structural characterization, by two-dimensional NMR spectroscopy and fast-atom-bombardment mass spectrometry, of a highly acylated trirhamnoside from Mezzettialeptopoda (Annonaceae)

3. Novel Cytotoxic Acylated Oligorhamnosides from Mezzettia leptopoda

4. Structure–Activity Relationship Study of the Cleistriosides and Cleistetrosides for Antibacterial/Anticancer Activity

5. Synthesis of Several Cleistrioside and Cleistetroside Natural Products via a Divergent De Novo Asymmetric Approach

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