An unexpected reaction in the lactamisation of 13-azido-13-deoxy-(9S)-9-dihydroerythronolide a seco-acid derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Chiral synthesis of polyketide-derived natural products. 27. Stereoselective synthesis of erythronolide A via an extremely efficient macrolactonization by the modified Yamaguchi method
2. Stereoselective synthesis of erythronolide a by extremely efficient lactonization based on conformational adjustment and high activation of seco-acid1
3. Synthesis of erythronolide a via a very efficient macrolactonization under usual acylation conditions with the Yamaguchi reagent
4. Asymmetric total synthesis of erythromycin. 2. Synthesis of an erythronolide A lactone system
5. Synthetic studies of erythromycins. II. Enantiospecific synthesis of A C-10-C-13 segment of erythronolide a from D-ribose
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1. Lactone and Lactam Formation;Comprehensive Organic Transformations;2018-02-28
2. 2-Pyridinethiol;Encyclopedia of Reagents for Organic Synthesis;2007-03-15
3. From ( E )- and ( Z )-ketoximes to N -sulfenylimines, ketimines or ketones at will. Application to erythromycin derivatives;Tetrahedron Letters;2004-07
4. Hybrids of macrolides and nucleobases or nucleosides;Tetrahedron Letters;2000-04
5. Reduction of Azides to Amines Mediated by Tin Bis(1,2-benzenedithiolate);Organic Letters;2000-01-20
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