Seijiro Hosokawa

准教授

Associate Professor 准教授, School of Advanced Science and Engineering

Websitehttp://researchers.waseda.jp/profile/ja.d533b8f418cab050e1eb91856cda3067.html

2649 Citations
29 h-Index

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1 Similar Profiles

Acetals Chemical Compounds

Biological Products Chemical Compounds

Cyclization Chemical Compounds

Stereoselectivity Chemical Compounds

Imides Chemical Compounds

Polyketides Chemical Compounds

Ciguatoxins Chemical Compounds

Alkylation Chemical Compounds

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Research Output 1994 2019

2649 Citations
29 h-Index
83 Article
2 Review article
1 Chapter

1 Citation (Scopus)

2-Isopropylbenzimidazole and 2-methylbenzimidazole as bulky proton sources: Stereoselective protonation and application to the synthesis of γ- and δ-lactones

Sengupta, A. & Hosokawa, S., 2019 Jan 31, In : Tetrahedron Letters. 60, 5, p. 411-414 4 p.

Research output: Contribution to journal › Article

Imides

Protonation

Lactones

Protons

Betula

Bioinspired Synthesis of the Central Core of Halichonadin H: The Passerini Reaction in a Hypothetical Biosynthesis of Marine Natural Products

Ichikawa, Y., Yamasaki, T., Nakanishi, K., Udagawa, Y., Hosokawa, S. & Masuda, T., 2019 Jan 1, In : Synthesis (Germany). 51, 11, p. 2305-2310 6 p.

Research output: Contribution to journal › Article

Terpenes

Biosynthesis

Biological Products

Cyanides

Formaldehyde

1 Citation (Scopus)

Synthesis of C3-C21 Segment of Aflastatin A Using Remote Asymmetric Induction Reactions

Murakoshi, S. & Hosokawa, S., 2019 Jan 1, (Accepted/In press) In : Organic Letters.

Research output: Contribution to journal › Article

Acetals

Alkylation

induction

synthesis

aflastatin A

1 Citation (Scopus)

Synthesis of the C1-C17 Segment of Bafilomycin N

Sato, H. & Hosokawa, S., 2019 Jan 1, In : Synlett. 30, 5, p. 577-580 4 p.

Research output: Contribution to journal › Article

Acetals

3-hydroxybutanal

semipinacol

1 Citation (Scopus)

Total Synthesis of PF1163B

Sengupta, A. & Hosokawa, S., 2019 Jan 1, In : Synlett. 30, 6, p. 709-712 4 p.

Research output: Contribution to journal › Article

Stereoselectivity

Depsipeptides

Imides

Polyketides

Acetals