One-Pot Synthesis of Functionalized 2,5-Dihydrofurans via an Amine-Promoted Petasis Borono–Mannich Reaction-Reference-Cited by-同舟云学术

One-Pot Synthesis of Functionalized 2,5-Dihydrofurans via an Amine-Promoted Petasis Borono–Mannich Reaction

Published:2013-11-14 Issue:23 Volume:15 Page:5944-5947
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Cui Chun-Xiao¹,Li Hui¹,Yang Xian-Jin¹,Yang Jun¹,Li Xiao-Qiang¹

Affiliation:

1. Key Lab for Advanced Materials & Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China, and Shanghai Institute of Organic Chemistry, Chinese Academy of Science, 345 Lingling Road, Shanghai 200032, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol402782f

Reference45 articles.

1. Stereoselective synthesis of 2,5-dihydrofurans by sequential SN2' cleavage of alkynyloxiranes and silver(I)-catalyzed cyclization of the allenylcarbinol products

2. Synthesis of the pseudopterane 2,5-furanocyclic ring system by [2,3] Wittig ring contraction of bridged furan and dihydrofuran propargylic ethers

3. An Expedient Route to Optically Pure 1-Butyne-3,4-diol from 2,5-Dihydrofuran

4. Synthesis of conjugated dienes from vinyl epoxides, vinyl acetonides and 2,5-dihydrofurans via zirconocene-mediated deoxygenation

5. Hydroxylated α-Vinylpyrrolidines from Sugar-Derived 2,5-Dihydrofurans. Synthesis of (1S,2S,8aR)-1,2-Dihydroxyindolizidine by Ring Closing Olefin Metathesis

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