Endo-benzonorbornen-2-ol as an efficient non-natural chiral auxiliary in the asymmetric aza-Diels–Alder reactions between cyclopentadiene and (1-phenylethyl)iminoacetates-Reference-Cited by-同舟云学术

Endo-benzonorbornen-2-ol as an efficient non-natural chiral auxiliary in the asymmetric aza-Diels–Alder reactions between cyclopentadiene and (1-phenylethyl)iminoacetates

Published:2014-10-16 Issue:101 Volume:4 Page:57768-57772
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Sousa Carlos A. D.,Maestro Miguel A.,Garcia-Mera Xerardo,Rodríguez-Borges José E.

Funder

FundaÃ§Ã£o para a CiÃancia e a Tecnologia

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA11143E

Reference34 articles.

1. J.Seyden-Penne, Chiral Auxiliaries and Ligands in Asymmetric Synthesis, John Wiley, New York, 1995

2. G.Roos, Compendium of Chiral Auxiliary Applications, ed. G. Roos, Academic Press, New York, 2002

3. Addition diastereoselective d'organozinciques sur le phenylglyoxalate de (−) menthyle

4. Preparation of an optically active prostaglandin intermediate via asymmetric induction

5. Enantioselective ring construction through asymmetric olefin-ketene cycloaddition. A highly enantiocontrolled approach to (-)-.alpha.-cuparenone and (+)-.beta.-cuparenone

Cited by 6 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. 40.1.1.3.3.6 Synthesis of Amines by Pericyclic Reactions Involving C=N Units (Update 2020);SOS Knowledge Updates 2020/1;2020

2. Mechanistic insights for the transprotection of tertiary amines with Boc2O via charged carbamates: access to both enantiomers of 2-azanorbornane-3-exo-carboxylic acids;Organic Chemistry Frontiers;2019

3. α-Imino Esters in Organic Synthesis: Recent Advances;Chemical Reviews;2017-06-12

4. Recent Contributions to Hetero Diels-Alder Reactions;Current Organic Chemistry;2016-07-28

5. On the scope of oxidation of tertiary amines: Meisenheimer rearrangements versus Cope elimination in 2-(cyanoethyl)-2-azanorbornanes;Organic Chemistry Frontiers;2016