Stereoselectivities of the intramolecular Diels-Alder reaction in the azanona- and azadecatriene series. Preparation of some polyhydroisoindoles, polyhydroisoquinolines, decahydropyrido[2,1-a]isoindoles and decahydro-2H-pyrido[1,2-b]isoquinolines-Reference-Cited by-同舟云学术

Stereoselectivities of the intramolecular Diels-Alder reaction in the azanona- and azadecatriene series. Preparation of some polyhydroisoindoles, polyhydroisoquinolines, decahydropyrido[2,1-a]isoindoles and decahydro-2H-pyrido[1,2-b]isoquinolines

Published:1998-08 Issue:33 Volume:54 Page:9529-9558
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Tsirk Anders,Gronowitz Salo,Hörnfeldt Anna-Britta

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference74 articles.

1. A stereoselective synthesis of dialkylaminomethyl substituted halobutadienes via amine induced ring-opening of thiophene-1,1-dioxides

2. Synthesis and Amine-Induced Ring-Opening of Silyl-Substituted Thiophene 1,1-Dioxides

3. Synthesis of substituted thiophene-1,1-dioxides and their ring-opening reactions with ω-unsaturated secondary amines; a synthetic route to azatrienes

4. Synthesis of substituted benzo[b]indolizidines and Benzo[b]-quinolizidines via ring-opening of 3-bromo-2,5-dimethylthiophene-1,1-dioxide

5. Introduction of Amino Alcohols in the Ring-Opening Reaction of 3-bromo-2,5-dimethylthiophene 1,1-dioxide. A short diastereoselective synthesis of substituted ‘tetrahydrobenzo[a]pyrrolizidines’ (= octahydro-1H-pyrrolo[2,1-a]isoindoles) usingL-prolinol

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1. Synthesis of Hexahydro-1H-isoindole Derivatives from Arylacyl Bromides via Homoallenic Bromohydrins;The Journal of Organic Chemistry;2015-02-09

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