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Hiroko Matsukura

Researcher at Toho University

Publications -  49
Citations -  802

Hiroko Matsukura is an academic researcher from Toho University. The author has contributed to research in topics: Ring (chemistry) & Ether. The author has an hindex of 15, co-authored 49 publications receiving 787 citations.

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Organic synthesis at high pressure

TL;DR: In this article, the authors recommend that all synthetic chemists should always consider pressure as one of the routine variables available to them, along with temperature, solvent, reaction time, catalysts, and so forth.
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An efficient strategy for the iterative synthesis of a trans-fused polytetrahydropyran ring system via SmI2-induced reductive intramolecular cyclization

TL;DR: In this article, a trans-fused polytetrahydropyran ring system was developed, which involves SmI2-induced reductive intramolecular cyclization of an aldehyde and a β-alkoxy acrylate as the key step.
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Efficient strategy for the iterative synthesis of trans-fused polycyclic ether via SmI2-induced reductive intramolecular cyclization

TL;DR: In this article, a new iterative method involves SmI 2 -induced reductive intramolecular cyclization of an aldehyde and a β-alkoxy acrylate as the key step, producing a 2,3- trans-tetrahydropyran or oxepane ring.
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Total synthesis of hemibrevetoxin B

TL;DR: The total synthesis of hemibrevetoxin B was stereoselectively accomplished based on a novel double rearrangement-ring expansion of a 6,6-membered ether to a 7,7-embered ether, an exclusive 6- endo -cyclization of hydroxy styrylepoxide, and a direct introduction of a C-4 unit as the side chain on the A-ring as mentioned in this paper.
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Stereoselective synthesis of six- and seven-membered ether rings based on the ring expansion

TL;DR: In this paper, six-and seven-membered ether rings were synthesized based on the rearrangement of the cyclic ether with the simultaneous ring expansion, which was called ring expanded ether.