On the choice of Lewis acids for the Prins reaction; two total syntheses of (±)-Civet-Reference-Cited by-同舟云学术

On the choice of Lewis acids for the Prins reaction; two total syntheses of (±)-Civet

Published:2011-07 Issue:27-28 Volume:67 Page:5107-5124
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Chio Freda K.,Warne Julie,Gough Damien,Penny Mark,Green (née Martinović) Sasa,Coles Simon J.,Hursthouse Mike B.,Jones Peter,Hassall Lorraine,McGuire Thomas M.,Dobbs Adrian P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference56 articles.

1. Synthesis of tetrahydropyrans and related heterocycles via prins cyclization; extension to aza-prins cyclization

2. Iron(III)-Promoted Aza-Prins-Cyclization: Direct Synthesis of Six-Membered Azacycles

3. The Aza-Silyl-Prins Reaction: A Novel Method for the Synthesis ofTrans-2,6-Tetrahydropyridines

4. A detailed investigation of the aza-Prins reaction

5. Formal Alkyne Aza-Prins Cyclization: Gold(I)-Catalyzed Cycloisomerization of Mixed N,O-Acetals Generated from Homopropargylic Amines to Highly Substituted Piperidines

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