Synthesis of β -prolinols via [3+2] cycloaddition and one-pot programmed reduction: Valuable building blocks for polyheterocycles-Reference-Cited by-同舟云学术

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Synthesis of β -prolinols via [3+2] cycloaddition and one-pot programmed reduction: Valuable building blocks for polyheterocycles

Published:2016-12 Issue:51 Volume:57 Page:5777-5780
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Li Jundong,Lin Na,Yu Lei,Zhang Yandong

Funder

Natural Science Foundation of China

SRF

FRFCU

NFFTBS

Beijing National Laboratory for Molecular Science

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference69 articles.

1. Stereoselective Rearrangement of (Trifluoromethyl)prolinols to Enantioenriched 3-Substituted 2-(Trifluoromethyl)piperidines

2. Access to Optically Active 3-Substituted Piperidines by Ring Expansion of Prolinols and Derivatives

3. Short asymmetric synthesis of (S,S)-PDP using l-prolinol derivative as economic starting material

4. Prolinol-based nucleoside phosphonic acids: new isosteric conformationally flexible nucleotide analogues

5. Enantioselective ring expansion of prolinol derivatives. Two formal syntheses of (−)-swainsonine

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2. Synthesis of the Hexahydropyrrolo-[3,2-c]-quinoline Core Structure and Strategies for Further Elaboration to Martinelline, Martinellic Acid, Incargranine B, and Seneciobipyrrolidine;Molecules;2021-01-11

3. Planar chiral [2.2]paracyclophane-based phosphine–phenols: use in enantioselective [3 + 2] annulations of allenoates and N-tosylimines;Organic & Biomolecular Chemistry;2018

4. Cycloaddition/annulation strategies for the construction of multisubstituted pyrrolidines and their applications in natural product synthesis;Organic Chemistry Frontiers;2018

5. Seven-Membered Rings;Progress in Heterocyclic Chemistry;2017

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