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5 in total

1. Synthesis of Spirocyclic Ethers by Enantioselective Copper-Catalyzed Carboetherification of Alkenols.

Authors: Shuklendu D Karyakarte; Chanchamnan Um; Ilyas A Berhane; Sherry R Chemler
Journal: Angew Chem Int Ed Engl Date: 2018-09-03 Impact factor: 15.336

2. Enantioselective Organocopper-Catalyzed Hetero Diels-Alder Reaction through in Situ Oxidation of Ethers into Enol Ethers.

Authors: Ahmet Yesilcimen; Na-Chuan Jiang; Felix H Gottlieb; Masayuki Wasa
Journal: J Am Chem Soc Date: 2022-04-05 Impact factor: 16.383

3. Tandem C-H oxidation/cyclization/rearrangement and its application to asymmetric syntheses of (-)-brussonol and (-)-przewalskine E.

Authors: Zhi-Wei Jiao; Yong-Qiang Tu; Qing Zhang; Wen-Xing Liu; Shu-Yu Zhang; Shao-Hua Wang; Fu-Min Zhang; Sen Jiang
Journal: Nat Commun Date: 2015-06-17 Impact factor: 14.919

4. Stereoselective construction of sterically hindered oxaspirocycles via chiral bidentate directing group-mediated C(sp³)-O bond formation.

Authors: Yechan Kim; Seoung-Tae Kim; Dahye Kang; Te-Ik Sohn; Eunyoung Jang; Mu-Hyun Baik; Sungwoo Hong
Journal: Chem Sci Date: 2017-11-27 Impact factor: 9.825

5. Highly diastereoselective synthesis of tricyclic fused-pyrans by sequential hydride shift mediated double C(sp³)-H bond functionalization.

Authors: Keiji Mori; Nobuaki Umehara; Takahiko Akiyama
Journal: Chem Sci Date: 2018-06-25 Impact factor: 9.825

5 in total

Organocatalytic asymmetric direct C(sp3)-H functionalization of ethers: a highly efficient approach to chiral spiroethers.

1. Synthesis of Spirocyclic Ethers by Enantioselective Copper-Catalyzed Carboetherification of Alkenols.

2. Enantioselective Organocopper-Catalyzed Hetero Diels-Alder Reaction through in Situ Oxidation of Ethers into Enol Ethers.

3. Tandem C-H oxidation/cyclization/rearrangement and its application to asymmetric syntheses of (-)-brussonol and (-)-przewalskine E.

4. Stereoselective construction of sterically hindered oxaspirocycles via chiral bidentate directing group-mediated C(sp3)-O bond formation.

5. Highly diastereoselective synthesis of tricyclic fused-pyrans by sequential hydride shift mediated double C(sp3)-H bond functionalization.

4. Stereoselective construction of sterically hindered oxaspirocycles via chiral bidentate directing group-mediated C(sp³)-O bond formation.

5. Highly diastereoselective synthesis of tricyclic fused-pyrans by sequential hydride shift mediated double C(sp³)-H bond functionalization.