Highly diastereoselective diels-alder reaction mediated by a chiral auxiliary derived from amino indanol: The role of conformation on diastereoselectivity-Reference-Cited by-同舟云学术

Highly diastereoselective diels-alder reaction mediated by a chiral auxiliary derived from amino indanol: The role of conformation on diastereoselectivity

Published:1995-10 Issue:42 Volume:36 Page:7619-7622
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Davies Ian W.,Senanayake Chris H.,Castonguay Laurie,Larsen Robert D.,Verhoeven Thomas R.,Reider Paul J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. The behavior of indene oxide in the ritter reaction: A simple route to cis-aminoindanol

2. Diastereoselective syn-epoxidation of 2-alkyl-4-enamides to epoxyamides: Synthesis of the Merck HIV-1 protease inhibitor epoxide intermediate

3. Highly enantioselective aldol reaction: development of a new chiral auxiliary from cis-1-amino-2-hydroxyindan

4. Asymmetric Diels-Alder cycloaddition reactions with chiral .alpha.,.beta.-unsaturated N-acyloxazolidinones

Cited by 53 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. Formation of Alkenes by Diels-Alder Reactions;Comprehensive Organic Transformations;2018-02-28

2. Electrophilic Oxidation of Stereodefined Polysubstituted Silyl Ketone Aminals;European Journal of Organic Chemistry;2017-12-06

3. (1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol;Encyclopedia of Reagents for Organic Synthesis;2016-12-01

4. Benzoate dioxygenase fromRalstonia eutrophaB9 – unusual regiochemistry of dihydroxylation permits rapid access to novel chirons;Org. Chem. Front.;2014

5. Cycloadditions II;Key Chiral Auxiliary Applications;2014