Sequential Prins/Pinacol Strategy for the Stereoselective Synthesis of Spiro-β-tetralones-Reference-Cited by-同舟云学术

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Sequential Prins/Pinacol Strategy for the Stereoselective Synthesis of Spiro-β-tetralones

Published:2016-01-18 Issue:3 Volume:5 Page:411-416
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Reddy B. V. Subba¹,Raju N. Prudhvi¹²,Reddy B. Jagan Mohan²,Sridhar B.³

Affiliation:

1. Natural Product Chemistry; CSIR-Indian Institute of Chemical Technology; Tarnaka 500 007 India

2. Department of Organic Chemistry; Adikavi Nannaya University; Rajahmundry 533105 India

3. Laboratory of X-ray Crystallography; CSIR-Indian Institute of Chemical Technology; Tarnaka 500 007 India

Funder

UGC, New Delhi

Publisher

Wiley

Subject

Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajoc.201500445/fullpdf

Reference70 articles.

1. Prins-Type Cyclization Reactions in Natural Product Synthesis

2. Focused Update on the Prins Reaction and the Prins Cyclization

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Carbonyl and Imine Ene Reactions, Prins Reactions and Cyclizations, and Lewis Acid–Catalyzed Carbonyl Olefin Metathesis;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023

2. TMSOTf‐Promoted Synthesis of 4‐(2‐Aryl or 2‐Alkyl‐3,6‐dihydro‐2 H ‐pyran‐4‐yl)‐1,2,3,6‐tetrahydropyridine Derivatives;ChemistrySelect;2019-03-25

3. ChemInform Abstract: Sequential Prins/Pinacol Strategy for the Stereoselective Synthesis of Spiro-β-tetralones.;ChemInform;2016-07

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