Stereoselective Synthesis of Hexahydro-1H-spiro[isoquinoline-4,4′-pyran] Scaffolds through an Intramolecular Prins Cascade Process-Reference-Cited by-同舟云学术

Stereoselective Synthesis of Hexahydro-1H-spiro[isoquinoline-4,4′-pyran] Scaffolds through an Intramolecular Prins Cascade Process

Published:2014-12-02 Issue:1 Volume:80 Page:653-660
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Subba Reddy B. V.¹,Medaboina Durgaprasad¹,Sridhar B.¹

Affiliation:

1. Natural Product Chemistry and ‡Laboratory of X-ray Crystallography, Academy of Scientific and Innovative Research, Indian Institute of Chemical Technology, Hyderabad 500 007, India

Funder

Council of Scientific and Industrial Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo5023926

Reference65 articles.

1. An Imine Addition/Ring-Closing Metathesis Approach to the Spirocyclic Core of Halichlorine and Pinnaic Acid

2. Transannular Nitrone Cycloaddition. A Stereocontrolled Entry to the Spirocyclic Core of Pinnaic Acid

3. Total Synthesis of SR 121463 A, a Highly Potent and Selective Vasopressin V2 Receptor Antagonist

4. Highly Diastereoselective Formation of Spirocyclic Compounds via 1,5-Hydrogen Transfer: A Total Synthesis of (−)-Erythrodiene

5. Synthesis and DNA Binding of Spirocyclic Model Compounds Related to the Neocarzinostatin Chromophore

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