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Shun-ichiro Hachiya

Observed names: S. HACHIYA, S. Hachiya, Shun-Ichiro Hachiya, Shun-ichiro HACHIYA, Shunichiro Hachiya, Shun‐Ichiro Hachiya
OpenAlex ID: A5001007567
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 3. Synthesis of C27-C36 SubunitviaCompletely StereoselectiveC-Glycosylation to the F Ring
1994 · K. Horita, Y. Sakurai, et al. · Synlett · 41
Applications of crotyldiisopinocampheylboranes in synthesis: a formal total synthesis of (+)-calyculin A
2001 · Oren P. Anderson, Anthony G.M. Barrett, et al. · Canadian Journal of Chemistry · 40
Discovery of N -[2-Hydroxy-6-(4-methoxybenzamido)phenyl]-4- (4-methyl-1,4-diazepan-1-yl)benzamide (Darexaban, YM150) as a Potent and Orally Available Factor Xa Inhibitor
2011 · Fukushi Hirayama, Hiroyuki Koshio, et al. · Journal of Medicinal Chemistry · 35
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 1. Stereoselective Synthesis of the C1-C13 FragmentviaConstruction of the B and A Rings by Kinetically and thermodynamically Controlled Intramolecular Michael Reactions.
1994 · K. Horita, S. Hachiya, et al. · Synlett · 33
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 6. Synthesis of the C1-C15 Unit via Stereoselective Construction of the B and A Rings by Kinetically and Thermodynamically Controlled Michael Reactions with the Aid of Computational Search for Dominant Conformers.
1997 · Kiyoshi HORITA, Shun-ichiro HACHIYA, et al. · Chemical and Pharmaceutical Bulletin · 20
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Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge 5. A Highly Concise and Efficient Synthesis of the C37~C54 Tricyclic JKL-Ring Part
1996 · Kiyoshi Horita, Shun-ichiro Hachiya, et al. · Heterocycles · 20
Design, synthesis and biological activity of YM-60828 derivatives: potent and orally-Bioavailable factor Xa inhibitors based on naphthoanilide and naphthalensulfonanilide templates
2002 · Fukushi Hirayama, Hiroyuki Koshio, et al. · Bioorganic & Medicinal Chemistry · 19
Synthetic studies of halichondrin B, an antitumor polyether macrolide isolated from a marine sponge. 8. Synthesis of the lactone part (C1C36) via horner-emmons coupling between C1C15 and C16C36 fragments and Yamaguchi lactonization
1997 · Kiyoshi Horita, Masaaki Nagasawa, et al. · Tetrahedron Letters · 19
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 4. Synthesis of the C37-C54 SubunitviaStereoselective Construction of Three Consecutive J, K, and L Rings
1994 · K. Horita, Y. Sakurai, et al. · Synlett · 16
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 2. Efficient Synthesis of C16-C26 FragmentsviaConstruction of the D Ring by a Highly Stereocontrolled Iodoetherification
1994 · K. Horita, M. Nagasawa, et al. · Synlett · 15
Synthesis, Characterization and Reactions of Enantiomerically Pure ‘Winged’ Spirane Porphyrazines
2000 · Shun-ichiro Hachiya, Andrew S. Cook, et al. · Tetrahedron · 13
Chiral synthesis of polyketide-derived natural products. 44. Large Laboratory scale Synthesis of (2S,3S)-2-(4-Methoxybenzyloxy)-3,4-O-(3-pentylidene)-1,3,4-butantriol, a Versatile Chiral Building Block in Natural Product Synthesis.
1994 · Kiyoshi HORITA, Youji SAKURAI, et al. · Chemical and Pharmaceutical Bulletin · 8
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ChemInform Abstract: Applications of Crotyldiisopinocampheylboranes in Synthesis: A Formal Total Synthesis of (+)‐Calyculin A.
2002 · Oren P. Anderson, Anthony G. M. Barrett, et al. · ChemInform
ChemInform Abstract: Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. Part 8. Synthesis of the Lactone Part (C1—C36) via Horner—Emmons Coupling Between C1—C15 and C16—C36 Fragments and Yamaguchi Lactonization.
1998 · K. HORITA, M. NAGASAWA, et al. · ChemInform
ChemInform Abstract: Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. Part 6. Synthesis of the C1—C15 Unit via Stereoselective Construction of the B and A Rings by Kinetically and Thermodynamically Controlled Michael Reactions with the Aid of Computational Search for Dominant Conformers.
1998 · K. HORITA, S. HACHIYA, et al. · ChemInform
ChemInform Abstract: Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. Part 5. A Highly Concise and Efficient Synthesis of the C37‐C54 Tricyclic JKL‐Ring Part.
1996 · K. HORITA, S. HACHIYA, et al. · ChemInform
ChemInform Abstract: Chiral Synthesis of Polyketide‐Derived Natural Products. Part 44. Large Laboratory Scale Synthesis of (2S,3S)‐2‐(4‐Methoxybenzyloxy)‐3,4‐ O‐(3‐pentylidene)‐1,3,4‐butantriol, a Versatile Chiral Building Block in Natural Product Synthesis.
1994 · K. HORITA, Y. SAKURAI, et al. · ChemInform
ChemInform Abstract: Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. Part 4. Synthesis of the C37‐C54 Subunit via Stereoselective Construction of Three Consecutive J, K, and L Rings.
1994 · K. HORITA, Y. SAKURAI, et al. · ChemInform
ChemInform Abstract: Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. Part 3. Synthesis of C27‐C36 Subunit via Completely Stereoselective C‐Glycosylation of the F Ring.
1994 · K. HORITA, Y. SAKURAI, et al. · ChemInform
ChemInform Abstract: Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. Part 1. Stereoselective Synthesis of the C1‐C13 Fragment via Construction of the B and A Rings by Kinetically and Thermodynamically Controlled Intramolecular Michael Reactions.
1994 · K. HORITA, S. HACHIYA, et al. · ChemInform
ChemInform Abstract: Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. Part 2. Efficient Synthesis of C16‐C26 Fragments via Construction of the D Ring by a Highly Stereocontrolled Iodoetherification.
1994 · K. HORITA, M. NAGASAWA, et al. · ChemInform
Works count: 21
Citation count: 279
H-index: 11
I10-index: 11
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