Transannular Diels–Alder Reactivities of 14-Membered Macrocylic Trienes and Their Relationship with the Conformational Preferences of the Reactants: A Combined Quantum Chemical and Molecular Dynamics Study-Reference-Cited by-同舟云学术

Transannular Diels–Alder Reactivities of 14-Membered Macrocylic Trienes and Their Relationship with the Conformational Preferences of the Reactants: A Combined Quantum Chemical and Molecular Dynamics Study

Published:2012-06-06 Issue:12 Volume:77 Page:5371-5380
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Prathyusha V.¹,Ramakrishna S.¹,Priyakumar U. Deva¹

Affiliation:

1. Center for Computational Natural Sciences and Bioinformatics, International Institute of Information Technology, Hyderabad 500 032, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo300812q

Reference85 articles.

1. Transannular Diels-Alder reaction on macrocycles. A general strategy for the synthesis of polycyclic compounds

2. Synthesis of (-)-longithorone A: Using organic synthesis to probe a proposed biosynthesis

3. Insight into a natural Diels–Alder reaction from the structure of macrophomate synthase

4. Lovastatin Nonaketide Synthase Catalyzes an Intramolecular Diels−Alder Reaction of a Substrate Analogue

5. Total Synthesis of (−)-Solanapyrone A via Enzymatic Diels−Alder Reaction of Prosolanapyrone

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