Stereoselective Synthesis ofC-2-Methylene andC-2-Methyl α- and β-C-Glycosides from 2-C-Branched Glycals: Formal Total Synthesis of (-)-Brevisamide-Reference-Cited by-同舟云学术

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Stereoselective Synthesis ofC-2-Methylene andC-2-Methyl α- and β-C-Glycosides from 2-C-Branched Glycals: Formal Total Synthesis of (-)-Brevisamide

Published:2014-11-06 Issue:36 Volume:2014 Page:8085-8093
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Sudharani Chalapala,Venukumar Patteti,Sridhar Perali Ramu

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference58 articles.

1. Synthesis of Branched-Chain Sugars

2. Total Synthesis of (−)-Polycavernoside A: Suzuki–Miyaura Coupling Approach

3. (+)-Sorangicin A: evolution of a viable synthetic strategy

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1. Recent Advances in the Synthesis and Application of C-2-Formyl Glycals;Synthesis;2023-03-30

2. A simple and efficient pathway for the total synthesis of marine natural products: bengamide E and 5-epi-bengamide E;Organic & Biomolecular Chemistry;2023

3. Regioselective Anomeric O ‐Benzyl Deprotection in Carbohydrates;European Journal of Organic Chemistry;2021-11-04

4. Synthesis of Carbon-Branched Sugars Involving an Unprecedented 1,5- or 1,6-Alkyl Transposition Reaction;European Journal of Organic Chemistry;2019-07-23

5. [3, 3]-Sigmatropic Rearrangement as a Powerful Synthetic Tool on Skeletal Modification of Unsaturated Sugars;Coupling and Decoupling of Diverse Molecular Units in Glycosciences;2017-11-21

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