Isolation of phytochemicals from <i>Dolichandrone atrovirens</i> followed by semisynthetic modification of ixoside via azomethine ylide cycloaddition; computational approach towards chemo-selection-Reference-Cited by-同舟云学术

Isolation of phytochemicals from Dolichandrone atrovirens followed by semisynthetic modification of ixoside via azomethine ylide cycloaddition; computational approach towards chemo-selection

Published:2022-02-06 Issue: Volume: Page:1-10
ISSN:1478-6419
Container-title:Natural Product Research
language:en
Short-container-title:Natural Product Research

Author:

Singh Meenakshi¹,Hirlekar Bhakti Umesh¹^ORCID,Mondal Shagufta¹,Pant Suyash¹,Dhaked Devendra K.¹,Ravichandiran V.¹,Hazra Abhijit¹^ORCID,Bharitkar Yogesh P.¹^ORCID

Affiliation:

1. National Institute of Pharmaceutical Education and Research (NIPER), Chunilal Bhawan, Kolkata, India

Publisher

Informa UK Limited

Subject

Organic Chemistry,Plant Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/14786419.2022.2037084

Reference44 articles.

1. 2α-Hydroxymicromeric acid, a pentacyclic triterpene from Terminalia chebula

2. Isolation of β-Sitosterol-D-Glucoside from Groundnut Phospholipids

3. Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection

4. Chemistry of withaferin-A: chemo, regio, and stereoselective synthesis of novel spiro-pyrrolizidino-oxindole adducts of withaferin-A via one-pot three-component [3+2] azomethine ylide cycloaddition and their cytotoxicity evaluation

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1. A new acylated triterpene glycoside and cytotoxic constituents from Dolichandrone serrulata (Wall. ex DC.) Seem;Natural Product Research;2024-01-23

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