Model reactions for sterically controlled syntheses of cyclohex-2-enones with 4,4- or 5,5-quaternary centers: a direct chiral synthesis of 4-allyl-4-cyanocyclohex-2-enone from the anion of (+)-tricarbonyl(5-cyano-2-methoxycyclohexa-1,3-diene)iron-Reference-Cited by-同舟云学术

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Model reactions for sterically controlled syntheses of cyclohex-2-enones with 4,4- or 5,5-quaternary centers: a direct chiral synthesis of 4-allyl-4-cyanocyclohex-2-enone from the anion of (+)-tricarbonyl(5-cyano-2-methoxycyclohexa-1,3-diene)iron

Published:1985-03 Issue:5 Volume:50 Page:712-714
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Birch Arthur J.,Kelly Lawrence F.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00205a038

Cited by 20 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. Organometallic Complexes of Dienes and Polyenes;PATAI'S Chemistry of Functional Groups;2009-12-15

2. Synthetic applications of cationic iron and cobalt carbonyl complexes;Dalton Transactions;2009

3. Selective Synthesis and Reactivity of η5-Arylcyclohexadienyliron Complexes;Chemistry - A European Journal;2007-05-18

4. Polyfunctional Electrophilic Multihapto‐Organometallics for Organic Synthesis;Handbook of Functionalized Organometallics;2005-08-23

5. Diastereofacially selective enolate Claisen rearrangements of [4−7-η4-(1-acyloxy-2,4,6-octatrienyl)]tricarbonyliron complexes;Tetrahedron Letters;1997-01

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