Deleterious effect of 7-methyl group on glycosylation of 2-naphthols-Reference-Cited by-同舟云学术

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Deleterious effect of 7-methyl group on glycosylation of 2-naphthols

Published:2015-08 Issue:34 Volume:71 Page:5610-5619
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Mitra Prithiba,Mandal Subhajit,Chakraborty Soumen,Mal Dipakranjan

Funder

Indian Institute of Technology Kharagpur

Department of Science and Technology, Ministry of Science and Technology

(SR/S1/OC-24/2011)

Council of Scientific and Industrial Research

(02(0183)/14/EMR-II)

University Grants Commission

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Mayamycin, a Cytotoxic Polyketide from a Streptomyces Strain Isolated from the Marine Sponge Halichondria panicea

2. Synthesis Study toward Mayamycin

3. Angucycline C5 Glycosides: Regio- and Stereocontrolled Synthesis and Cytotoxicity

4. Total Synthesis of (±)-O-Methyl PD 116740

5. Dorsch, W. A. Doctoral dissertation, 2002. Retrieved from ProQuest/UMI Dissertations and Theses (UMI Number 3058967).

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1. Hauser–Kraus, Sammes, Staunton–Weinreb, and Tamura Annulations;Organic Reactions;2021-09-17

2. Aromatic Substitution;Organic Reaction Mechanisms Series;2019-03-07

3. [4 + 2] Annulation With Nonactivated Phthalides (Sammes Annulation);Anionic Annulations in Organic Synthesis;2019

4. A Representative Synthetic Route for C5 Angucycline Glycosides: Studies Directed toward the Total Synthesis of Mayamycin;The Journal of Organic Chemistry;2018-01-16

5. C-Glycosylation of Substituted β-Naphthols with Trichloroacetimidate Glycosyl Donors;Synthesis;2018-01-03

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