The bicyclo[3.3.1]nonane solution to the problem of vicinal stereochemical control at a substituted cyclohexane ring. A total synthesis of dl-erythrojuvabione-Reference-Cited by-同舟云学术

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The bicyclo[3.3.1]nonane solution to the problem of vicinal stereochemical control at a substituted cyclohexane ring. A total synthesis of dl-erythrojuvabione

Published:1984-07 Issue:14 Volume:49 Page:2615-2618
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Schultz Arthur G.,Dittami James P.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00188a020

Cited by 11 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. Olefins Conjugated to Carbonyl, Nitrile, Nitro;Inorganic Reactions and Methods;2007-05-29

2. II. Monocyclic Sesquiterpenes;Total Synthesis of Natural Products;2007-02-20

3. Enantiospecific synthesis of functionalised bicyclo[3.3.1]nonanes from 10-bromocarvones via tandem intermolecular alkylation-intramolecular Michael addition sequence;Arkivoc;2003-02-14

4. Application of the Novel Tandem Process Diels-Alder Reaction/Ireland-Claisen Rearrangement to the Synthesis of rac-Juvabione and rac-Epijuvabione;Helvetica Chimica Acta;2000-09-06

5. Enantioselective intramolecular cyclizations of prochiral cyclohexanones using chiral lithium amide bases;Chemical Communications;1998

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