1. A Novel Aryl Migration from Silicon to Carbon: An Efficient Approach to Asymmetric Synthesis of a-Aryl β-Hydroxy Cyclic Amines and Silanols
Katsuhiko Tomooka, Atsuo Nakazaki, Takeshi Nakai
J. Am. Chem. Soc. 2000, 122, 408-409.
2. Synthesis of the Hydroazulene Portion of Guanacastepene A from the Cyclopentannelation Reaction
Atsuo Nakazaki, Utpal Sharma, Marcus A. Tius
Org. Lett. 2002, 4, 3363-3366.
3. Remote Asymmetric Induction with Vinylketene Silyl N,O-Acetal
Shin-ichi Shirokawa, Masato Kamiyama, Tomoaki Nakamura, Masakazu Okada, Atsuo Nakazaki, Seijiro Hosokawa, Susumu Kobayashi
J. Am. Chem. Soc. 2004, 126, 13604-13605.
4. Stereoselective 1,5-Rearrangement of Vinylketene-N,O-acetals: Novel Vinylogous Ferrier Reaction
Masaharu Inui, Seijiro Hosokawa, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron Lett. 2005, 46, 3245-3248.
5. Stereoselective Synthesis of Functionalized Spiro[4.5]decanes by Claisen Rearrangement of Bicyclic Dihydropyrans
Atsuo Nakazaki, Hiroshi Miyamoto, Kazuki Henmi, Susumu Kobayashi
Synlett 2005, 1417-1420.
6. Enantioselective Total Synthesis of Convolutamydines B and E
Tomoaki Nakamura, Shin-ichi Shirokawa, Seijiro Hosokawa, Atsuo Nakazaki, Susumu Kobayashi
Org. Lett. 2006, 8, 677-679.
7. Total Synthesis of (-)-Neoechinulin A
Toshiaki Aoki, Shinji Kamisuki, Masaaki Kimoto, Kensuke Ohnishi, Yoichi Takakusagi, Kouji Kuramochi, Yoshifumi Takeda, Atsuo Nakazaki, Kenji Kuroiwa, Takashi Ohuchi, Fumio Sugawara, Takao Arai, Susumu Kobayashi
Synlett 2006, 677-680.
8. Asymmetric Retro-[1,4] Brook Rearrangement and Its Stereochemical Course at Silicon
Atsuo Nakazaki, Takeshi Nakai, Katsuhiko Tomooka
Angew. Chem. Int. Ed. 2006, 45, 2235-2238.
9. Highly Diastereoselective One-Pot Synthesis of Spirocyclic Oxindoles through Intramolecular Ullmann Coupling and Claisen Rearrangement
Hiroshi Miyamoto, Yoichiro Okawa, Atsuo Nakazaki, Susumu Kobayashi
Angew. Chem. Int. Ed. 2006, 45, 2274-2277.
10. Stereoselective Total Synthesis of (±)-a-Vetispirene, (±)-Hinesol, and (±)-b-Vetivone Based on a Claisen Rearrangement
Atsuo Nakazaki, Tomohiro Era, Yuko Numada, Susumu Kobayashi
Tetrahedron 2006, 62, 6264-6271.
11. Synthesis and Absolute Configuration of (+)-Pseudodeflectusin: Structural Revision of Aspergione B
Fumiyo Saito, Kouji Kuramochi, Atsuo Nakazaki, Yoshiyuki Mizushina, Fumio Sugawara, Susumu Kobayashi
Eur. J. Org. Chem. 2006, 4796-4799.
12. Claisen Rearrangement Strategy in Alkenyl Dihydropyran Leading to Total Synthesis of (+)-a-Vetispirene and (ｰ)-Agarospirol
Atsuo Nakazaki, Susumu Kobayashi
Chem. Lett. 2007, 36, 42-43.
13. Highly Stereoselective Construction of Spiro[4.5]decanes by SmI2-Promoted Ketyl Radical Mediated Tandem Cyclization
Masaharu Inui, Atsuo Nakazaki, Susumu Kobayashi
Org. Lett. 2007, 9, 469-472.
14. Synthetic Study on Telomerase Inhibitor, D8646-2-6: Synthesis of the Key Intermediate using Sn(OTf)2 or Sc(OTf)3 Mediated Aldol-type Reaction and Stille Coupling
Akira Kanai, Yoshifumi Takeda, Kouji Kuramochi, Atsuo Nakazaki, Susumu Kobayashi
Chem. Pharm. Bull. 2007, 55, 495-499.
15. Total Synthesis of Khafrefungin Using Highly Stereoselective Vinylogous Mukaiyama Aldol Reaction
Shin-ichi Shirokawa, Mariko Shinoyama, Isao Ooi, Seijiro Hosokawa, Atsuo Nakazaki, Susumu Kobayashi
Org. Lett. 2007, 9, 849-852.
16. Total Synthesis of (±)-Debromoflustramine B and E and (±)-Debromoflustramide B Based on One-pot Intramolecular Ullmann Coupling and Claisen Rearrangement
Hiroshi Miyamoto, Yoichiro Okawa, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron Lett. 2007, 48, 1805-1808.
17. Total Synthesis of (±)-Gleenol and (±)-Axenol via a Functionalized Spiro[4.5]decane
Atsuo Nakazaki, Tomohiro Era, Susumu Kobayashi
Chem. Pharm. Bull. 2007, 55, 1606-1609.
18. Structure-activity Relationships of Neoechinulin A Analogues with Cytoprotection against Peroxynitrite-induced PC12 Cell Death
Kuniaki Kimoto, Toshiaki Aoki, Yasushi Shibata, Shinji Kamisuki, Fumio Sugawara, Kouji Kuramochi, Atsuo Nakazaki, Susumu Kobayashi, Kenji Kuroiwa, Nobuo Watanabe, Takao Arai
J. Antibiotics 2007, 60, 614-621.
19. Synthetic Study of Diversifolin: The Construction of 11-Oxabicyclo[6.2.1]undec-3-ene Core Using Ring Closing Metathesis
Tomoaki Nakamura, Motoko Oshida, Tomoko Nomura, Atsuo Nakazaki, Susumu Kobayashi
Org. Lett. 2007, 9, 5533-5536.
20. A PhSeCl-mediated Allylic Oxidation of Prenyl Moiety: A Convenient Method for the Construction of 3-Isopenten-2-ol Unit
Motoko Oshida, Tomoaki Nakamura, Atsuo Nakazaki, Susumu Kobayashi
Chem. Pharm. Bull. 2008, 56, 404-406.
21. Stereocontrolled Total Synthesis of (–)-Gleenol Using Claisen Rearrangement of Sterically Congested Dihydropyran
Atsuo Nakazaki, Tomohiro Era, Susumu Kobayashi
Chem. Lett. 2008, 37, 770-771.
22. Stereoselective 1,4-Phenyl Migration from Silicon to Carbon in a-Siloxy Cyclic Acetal Systems: A Concise Synthesis of 1,2-cis Phenyl C-Glycoside and Enantioenriched Silanol
Atsuo Nakazaki, Junji Usuki, Katsuhiko Tomooka
Synlett 2008, 2064-2068.
23. Efficient One-cycle Affinity Selection of Binding Proteins or Peptides Specific for a Small-molecule Using a T7 Phage Display Pool
Yoichi Takakusagi, Kouji Kuramochi, Manami Takagi, Tomoe Kusayanagi, Daisuke Manita, Hiroko Ozawa, Kanako Iwakiri, Kaori Takakusagi, Yuka Miyano, Atsuo Nakazaki, Susumu Kobayashi, Fumio Sugawara, Kengo Sakaguchi
Bioorg. Med. Chem. 2008, 16, 9837-9846.
24. Synthesis of Neoechinulin A and Derivatives
Kouji Kuramochi, Toshiaki Aoki, Atsuo Nakazaki, Shinji Kamisuki, Masahiro Takeno, Kensuke Ohnishi, Kuniaki Kimoto, Nobuo Watanabe, Takashi Kamakura, Takao Arai, Fumio Sugawara, Susumu Kobayashi
Synthesis 2008, 3810-3818.
25. Synthesis and Biological Activities of Neoechinulin A Derivatives: New Aspects of Structure-activity Relationships for Neoechinulin A
Kouji Kuramochi, Kensuke Ohnishi, Satoshi Fujieda, Mitsuhiro Nakajima, Yoshihiko Saitoh, Nobuo Watanabe, Toshifumi Takeuchi, Atsuo Nakazaki, Fumio Sugawara, Takao Arai, Susumu Kobayashi
Chem. Pharm. Bull. 2008, 56, 1738-1743..
26. Synthetic Study of (–)-Norzoanthamine: Construction of ABC Ring Moiety
Yoshihisa Murata, Daisuke Yamashita, Katsushi Kitahara, Yohei Minasako, Atsuo Nakazaki, Susumu Kobayashi
Angew. Chem. Int. Ed. 2009, 48, 1400-1403.
27. Total Synthesis of (–)-Norzoanthamine
Daisuke Yamashita, Yoshihisa Murata, Naotsuka Hikage, Ken-ichi Takao, Atsuo Nakazaki, Susumu Kobayashi
Angew. Chem. Int. Ed. 2009, 48, 1404-1406.
28. A Switch of Facial Selectivities Using a-Heteroatom-substituted Aldehydes in the Vinylogous Mukaiyama Aldol Reaction
Mariko Shinoyama, Shin-ichi Shirokawa, Atsuo Nakazaki, Susumu Kobayashi
Org. Lett. 2009, 11, 1277-1280.
29. Total Synthesis of (–)-Flustramine B Based on One-Pot Intramolecular Ullmann Coupling and Claisen Rearrangement
Tomohiro Hirano, Kanako Iwakiri, Hiroshi Miyamoto, Atsuo Nakazaki, Susumu Kobayashi
Heterocycles 2009, 79, 805-820.
30. Total Synthesis of (–)-Diversifolin
Tomoaki Nakamura, Kazuma Tsuboi, Motoko Oshida, Tomoko Nomura, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron Lett. 2009, 50, 2835-2839.
31. Synthetic Study of Fomitellic Acids: Construction of the AB Ring Moiety
Makoto Yamaoka, Yuichi Fukatsu, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron Lett. 2009, 50, 3849-3852.
32. Claisen Rearrangement Using Bicyclic 2-[(Z)-Alkenyl]dihydropyran: Stereoselective Synthesis of trans-Substituted Spiro[4.5]decane
Atsuo Nakazaki, Susumu Kobayashi
Synlett 2009, 1605-1608.
33. Stereocontrolled Total Synthesis of Antimalarial (+)-Axisonitrile-3
Keiji Tamura, Atsuo Nakazaki, Susumu Kobayashi
Synlett 2009, 2449-2452.
34. Total Synthesis of Fomitellic Acid B
Makoto Yamaoka, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron Lett. 2009, 50, 6764-6768.
35. Rate Enhancement by Water in a TiCl4-mediated Stereoselective Vinylogous Mukaiyama Aldol Reaction
Makoto Yamaoka, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron Lett. 2010, 51, 287-289.
36. Total Synthesis of (+)-Cacospongionolide B
Motoko Oshida, Misaki Ono, Atsuo Nakazaki, Susumu Kobayashi
Heterocycles 2010, 80, 313-328.
37. Second-generation Total Synthesis of (−)-Diversifolin
Kazuma Tsuboi, Tomoaki Nakamura, Takahiro Suzuki, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron Lett. 2010, 51, 1876-1879.
38. Synthesis and Neuroprotective Action of Optically Pure Neoechinulin A and Its Analogs
Toshiaki Aoki, Kensuke Ohnishi, Masaaki Kimoto, Satoshi Fujieda, Kouji Kuramochi, Toshifumi Takeuchi, Atsuo Nakazaki, Nobuo Watanabe, Fumio Sugawara, Takao Arai, Susumu Kobayashi
Pharmaceuticals 2010, 3, 1063-1069.
39. Synthesis of Pseudodeflectusin and Ustusorane C: Structural Revision of Aspergione A and B
Kouji Kuramochi, Fumiyo Saito, Atsuo Nakazaki, Toshifumi Takeuchi, Kazunori Tsubaki, Fumio Sugawara, Susumu Kobayashi
Biosci. Biotechnol. Biochem. 2010, 74, 1635-1640.
40. Unusual E-Selective Ring-Closing Metathesis to Form Eight-Membered Rings
Ryosuke Matsui, Kentaro Seto, Kazuhiro Fujita, Takahiro Suzuki, Atsuo Nakazaki, Susumu Kobayashi
Angew. Chem. Int. Ed. 2010, 49, 10068-10073.
41. The Second Generation Synthesis of (+)-Pseudodeflectusin
Yuna Sato, Kouji Kuramochi, Takahiro Suzuki, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron Lett. 2011, 52, 626-629.
42. Convergent Total Synthesis of (+)-TMC-151C Using Vinylogous Mukaiyama Aldol Reaction and Ring-Closing Metathesis
Ryosuke Matsui, Kentaro Seto, Yuna Sato, Takahiro Suzuki, Atsuo Nakazaki, Susumu Kobayashi
Angew. Chem. Int. Ed. 2011, 50, 680-683.
43. Stereoselective Vinylogous Mukaiyama Aldol Reaction of a-Haloenals
Yoichi Iwasaki, Ryosuke Matsui, Takahiro Suzuki, Atsuo Nakazaki, Susumu Kobayashi
Chem. Pharm. Bull. 2011, 59, 522-524.
44. Synthetic Study on Sespendole, an Indole Sesquiterpene Alkaloid: Stereocontrolled Synthesis of the Sesquiterpene Segment Bearing All Requisite Stereogenic Centers
Kumi Sugino, Atsuo Nakazaki, Minoru Isobe, Toshio Nishikawa
Synlett 2011, 647-650.
45. Different Modes of Cyclization in Zoanthamine Alkaloid System, Bisaminal versus Spiroketal Formation
Takahiro Nakajima, Daisuke Yamashita, Kaname Suzuki, Atsuo Nakazaki, Takahiro Suzuki, Susumu Kobayashi
Org. Lett. 2011, 13, 2980-2983.
46. Efficient synthesis of 3-O-thia-cPA and preliminary analysis of its biological activity toward autotoxin
Ryo Tanaka, Masaru Kato, Takahiro Suzuki, Atsuo Nakazaki, Emi Nozaki, Mari Gotoh, Kimiko Murakami-Murofushi, Susumu Kobayashi
Bioorg. Med. Chem. Lett. 2011, 21, 4180-4182.
47. Synthesis and Determination of the Relative Structure of Akaterpin, a Potent Inhibitor of PI-PLC
Hayato Hosoi, Nobuyuki Kawai, Hideki Hagiwara, Takahiro Suzuki, Atsuo Nakazaki, Ken-ichi Takao, Kazuo Umezawa, Susumu Kobayashi
Tetrahedron Lett. 2011, 52, 4961-4964.
48. Concise Synthesis of Deformylflustrabromine, a Marine Indole Alkaloid, through a Propargyl Dicobalt Hexacarbonyl Complex
Hisaaki Isaji, Atsuo Nakazaki, Minoru Isobe, Toshio Nishikawa
Chem. Lett. 2011, 40, 1079-1081.
49. Determination of the absolute structure of (+)-akaterpin
Hayato Hosoi, Nobuyuki Kawai, Hideki Hagiwara, Takahiro Suzuki, Atsuo Nakazaki, Ken-ichi Takao, Kazuo Umezawa, Susumu Kobayashi
Chem. Pharm. Bull. 2012, 60, 137-143.
50. Exploration of the binding proteins of perfluorooctane sulfonate by a T7 phage display screen
Yuka Miyano, Senko Tsukuda, Ippei Sakimoto, Ryo Takeuchi, Satomi Shimura, Noriyuki Takahashi, Tomoe Kusayanagi, Yoichi Takakusagi, Mami Okado, Yuki Matsumoto, Kaori Takakusagi, Toshifumi Takeuchi, Shinji Kamisuki, Atsuo Nakazaki, Keisuke Ohta, Masahiko Miura, Kouji Kuramochi, Yoshiyuki Mizushina, Susumu Kobayashi, Fumio Sugawara, Kengo Sakaguchi
Bioorg. Med. Chem. 2012, 20, 3985-3990.
51. Synthetic Studies on Pactamycin, a Potent Antitumor Antibiotic
Nobuyuki Matsumoto, Takashi Tsujimoto, Atsuo Nakazaki, Minoru Isobe, Toshio Nishikawa
RSC Advances, 2012, 2, 9448–9462.
52. Pharmacological evaluation of a novel cyclic phosphatidic acid derivative 3-S-cyclic phosphatidic acid (3-S-cPA)
Emi Nozaki, Mari Gotoh, Ryo Tanaka, Masaru Kato, Takahiro Suzuki, Atsuo Nakazaki, Harumi Hotta, Susumu Kobayashi, Kimiko Murakami-Murofushi
Bioorg. Med. Chem. 2012, 20, 3196-3201.
53. The antitumor agent doxorubicin binds to Fanconi anemia group F protein
Tomoe Kusayanagi, Senko Tsukuda, Satomi Shimura, Daisuke Manita, Kanako Iwakiri, Shinji Kamisuki, Yoichi Takakusagi, Toshifumi Takeuchi, Kouji Kuramochi, Atsuo Nakazaki, Kengo Sakaguchi, Susumu Kobayashi, Fumio Sugawara
Bioorg. Med. Chem. 2012, 20, 6248-6255.
54. Diastereoselective Synthesis of 3,3-Disubstituted Oxindoles from Atropisomeric N-Aryl Oxindole Derivatives
Atsuo Nakazaki, Ayako Mori, Susumu Kobayashi, Toshio Nishikawa
Tetrahedron Lett. 2012, 53, 7131-7134. DOI: 10.1016/j.tetlet.2012.10.092
55. Synthesis of Tetracyclic Indoline and Indolenine Derivatives Having b-Lactam Using Amphiphilic Reactivity of 2-Methylindolenine
Atsuo Nakazaki, Yukari Hara, Shigeo Kajii, Toshio Nishikawa
Heterocycles 2013, 87, 611-625.
56. Deprotection of the Methoxymethyl Group on 3-Spiro-2-oxindole under Basic Conditions
Atsuo Nakazaki, Kanako Iwakiri, Tomohiro Hirano, Takahiro Suzuki, Susumu Kobayashi
Chem. Pharm. Bull. 2013, 61, 587-591. DOI: 10.1248/cpb.c13-00068
57. Structural Study on a Naturally Occurring Terphenyl Quinone
Atsuo Nakazaki, Wen-Yu Huang, Kazushi Koga, Boon-ek Yingyongnarongkul, Jutatip Boonsombat, Yusuke Sawayama, Takashi Tsujimoto, Toshio Nishikawa
Biosci. Biotechnol. Biochem. 2013, 77, 1529-1532. DOI: 10.1271/bbb.130199
58. Stereoselective synthesis of spirocyclic oxindoles based on a one-pot Ullmann coupling/Claisen rearrangement and its application to the synthesis of a hexahydropyrrolo[2,3-b]indole alkaloid
Hiroshi Miyamoto, Tomohiro Hirano, Yoichiro Okawa, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron 2013, 69, 9481-9493. DOI: 10.1016/j.tet.2013.08.057
59. Synthesis of crambescin B carboxylic acid, a potent inhibitor of voltage-gated sodium channels
Atsuo Nakazaki, Yuki Ishikawa, Yusuke Sawayama, Mari Yotsu-Yamashita, Toshio Nishikawa
Org. Biomol. Chem. 2014, 12, 53-56. DOI: 10.1039/C3OB42017E
60. Synthetic study of spiroiridal triterpenoids: construction of functionalized spiro[4.5]decane skeleton using Claisen rearrangement of 2-(alkenyl)dihydropyran
Noriyuki Takanashi, Keiji Tamura, Takahiro Suzuki, Atsuo Nakazaki, Susumu Kobayashi
Tetrahedron Lett. 2015, 56, 327-330. DOI: 10.1016/j.tetlet.2014.11.078
61. Multimodal Biopanning of T7 Phage-displayed Peptide Reveals Angiomotin as a Potential Receptor of an Anti-angiogenic Macrolide Roxithromycin
Kaori Takakusagi, Yoichi Takakusagi, Takahiro Suzuki, Aya Toizaki, Aiko Suzuki, Yaichi Kawakatsu, Madoka Watanabe, Yukihiro Saito, Ryushi Fukuda, Atsuo Nakazaki, Susumu Kobayashi, Kengo Sakaguchi, Fumio Sugawara
Eur. J. Med. Chem. 2015, 90, 809-821. DOI: 10.1016/j.ejmech.2014.12.015
62. Unexpected Metal-Free Transformation of gem-Dibromomethylenes to Ketones under Acetylation Conditions
Rino Kimura, Yusuke Sawayama, Atsuo Nakazaki, Kazunori Miyamoto, Masanobu Uchiyama, Toshio Nishikawa
Chem. Asian J. 2015, 10, 1035-1041. DOI: 10.1002/asia.201403277.
63. Diastereoselective Synthesis of 3,3-Disubstituted Oxindoles from N-Aryl-3-Chlorooxindoles bearing C-N Axial Chirality via Nucleophilic Substitution
Atsuo Nakazaki, Keitaro Miyagawa, Toshio Nishikawa
Synlett 2015, 26, 1116-1120. DOI: 10.1055/s-0034-1380266
64. Synthesis of 1,5-Dioxaspiro[3.4]octane through Bromocation-induced Cascade Cyclization
Atsuo Nakazaki, Yoshiki Nakane, Yuki Ishikawa, Toshio Nishikawa
Heterocycles 2015, 91, 1157-1163. DOI: 10.3987/COM-15-13208
65. Synthesis of a C-N Axially Chiral N-Aryl Isatin through Asymmetric Intramolecular N-Arylation
Atsuo Nakazaki, Keitaro Miyagawa, Noriaki Miyata, Toshio Nishikawa
Eur. J. Org. Chem. 2015, 4603-4606. DOI: 10.1002/ejoc.201500593
66. Asymmetric Synthesis of Crambescin A–C Carboxylic Acids and Their Inhibitory Activity on Voltage-Gated Sodium Channels
Atsuo Nakazaki, Yoshiki Nakane, Yuki Ishikawa, Mari Yotsu-Yamashita, Toshio Nishikawa
Org. Biomol. Chem. 2016, 14, 5304-5309. DOI: 10.1039/C6OB00914J
67. A Divergent Approach to the Diastereoselective Synthesis of 3,3-Disubstituted Oxindoles from Atropisomeric N-Aryl Oxindole Derivatives
Atsuo Nakazaki, Ayako Mori, Susumu Kobayashi, Toshio Nishikawa
Chem. Asian J. 2016, 11, 3267-3274. DOI: 10.1002/asia.201601183
68. A Synthetic Strategy for Saxitoxin Skeleton by a Cascade Bromocyclization: Total Synthesis of (+)-Decarbamoyl-α-saxitoxinol
Sohei Ueno, Atsuo Nakazaki, Toshio Nishikawa
Org. Lett. 2016, 18, 6368-6371. DOI: 10.1021/acs.orglett.6b03262
69. Inhibition of veratridine-induced delayed inactivation of the voltage-sensitive sodium channel by synthetic analogs of crambescin B
Tadaaki Tsukamoto, Yukie Chiba, Atsuo Nakazaki, Yuki Ishikawa, Yoshiki Nakane, Yuko Cho, Mari Yotsu-Yamashita, Toshio Nishikawa, Minoru Wakamori, Keiichi Konoki
Bioorg. Med. Chem. Lett. 2017, 27, 1247-1251. DOI: 10.1016/j.bmcl.2017.01.054
70. Biomimetic Synthesis and Structural Revision of Chaxine B and its Analogues
Yushi Hirata, Atsuo Nakazaki, Hirokazu Kawagishi, Toshio Nishikawa
Org. Lett. 2017, 19, 560-563. DOI: 10.1021/acs.orglett.6b03724
71. Palladium-Catalyzed Cascade Wacker/Allylation Sequence with Allylic Alcohols Leading to Allylated Dihydropyrones
Wen-Yu Huang, Toshio Nishikawa, Atsuo Nakazaki
ACS Omega 2017, 2, 487-495. DOI: 10.1021/acsomega.7b00028
72. New regiocontrolled syntheses of pyrrolopyrazinones and its application to the synthesis of peramine
Yuta Yamamoto, Atsuo Nakazaki, Toshio Nishikawa
Tetrahedron 2017, 73, 3443-3451. DOI: 10.1016/j.tet.2017.05.004
73. Concise synthesis of a cyclopentane intermediate possessing all nitrogen functionalities for pactamycin
Nobuyuki Matsumoto, Atsuo Nakazaki, Toshio Nishikawa
Synlett 2017, 2303-2306. DOI: 10.1055/s-0036-1588495
74. De Novo Synthesis of Possible Candidates for the Inagami-Tamura Endogenous Digitalis-like Factor
Atsuo Nakazaki, Keiko Hashimoto, Ai Ikeda, Takahiro Shibata, Toshio Nishikawa
J. Org. Chem. 2017, 82, 9097-9111. DOI: 10.1021/acs.joc.7b01640
75. Synthetic Route to Oscillatoxin D and Its Analogues
Yoshihiko Nokura, Yusuke Araki, Atsuo Nakazaki, Toshio Nishikawa
Org. Lett. 2017, 19, 5992–5995. DOI: 10.1021/acs.orglett.7b03032
76. Synthesis of Dibromo Compounds Containing 2,6-Dioxabicyclo[3.1.1]heptane Similar to Core Moiety of Thromboxane A2
Yoshihiko Nokura, Atsuo Nakazaki, Toshio Nishikawa
Heterocycles 2018, 96, 127-136. DOI: 10.3987/COM-17-13814
77. Semi-synthesis and Structure-Activity Relationship of Neuritogenic Oleanene Derivatives
Linglin Bian, Shining Cao, Lihong Cheng, Atsuo Nakazaki, Toshio Nishikawa, Jianhua Qi
ChemMedChem 2018, 13, 1972-1977. DOI: 10.1002/cmdc.201800352
78. Toward a synthesis of fawcettimine-type Lycopodium alkaloids: stereocontrolled synthesis of a functionalized azaspirocycle precursor
Wen-Yu Huang, Toshio Nishikawa, Atsuo Nakazaki
J. Org. Chem. 2018, 83, 11108-11117. DOI: 10.1021/acs.joc.8b01719
79. Asymmetric Synthesis of the Aromatic Fragment of Sespendole
Yoshiki Ono, Atsuo Nakazaki, Kaori Ueki, Keiko Higuchi, Uraiwan Sriphana, Masaatsu Adachi, Toshio Nishikawa
J. Org. Chem. 2019, 84, 9750-9757. DOI: 10.1021/acs.joc.9b01597
80. Synthesis of Oxy-Functionalized Steroidal Skeletons via Mizoroki–Heck and Intramolecular Diels–Alder Reactions
Shogo Watanabe, Toshio Nishikawa, Atsuo Nakazaki
Org. Lett. 2019, 21, 7410-7414. DOI: 10.1021/acs.orglett.9b02716
81. Biomimetic Synthesis of Chaxine and its Related Compounds
Misaki Niki, Yushi Hirata, Atsuo Nakazaki, Jing Wu, Hirokazu Kawagishi, Toshio Nishikawa
J. Org. Chem. 2020, 85, 4848-4860. DOI: 10.1021/acs.joc.9b03482
82. Quantitative analysis of oxidized vitamin B1 metabolites generated by hypochlorous acid
Hitoshi Sasatsuki, Atsuo Nakazaki, Koji Uchida Takahiro Shibata
Free Radic. Biol. Med. 2020, 152, 197-206. DOI: 10.1016/j.freeradbiomed.2020.03.010
83. Studies toward the Synthesis of Chartelline C
Yoshiki Nakane, Atsuo Nakazaki, Toshio Nishikawa
J. Org. Chem. 2020, 85, 7534-7542. DOI: 10.1021/acs.joc.0c00643
84. Biosynthesis of Indole Diterpene Lolitrems: Radical-Induced Cyclization of an Epoxyalcohol Affording a Characteristic Lolitremane Skeleton
Yulu Jiang, Taro Ozaki, Mei Harada, Tadachika Miyasaka, Hajime Sato, Kazunori Miyamoto, Junichiro Kanazawa, Chengwei Liu, Jun-ichi Maruyama, Masaatsu Adachi, Atsuo Nakazaki, Toshio Nishikawa, Masanobu Uchiyama, Atsushi Minami, Hideaki Oikawa
Angew. Chem. Int. Ed. 2020, 59, 17996-18002. DOI: 10.1002/anie.202007280
総説
1. Claisen転位を鍵反応とする多官能性スピロ化合物の立体選択的構築と天然物合成への応用
中崎敦夫、小林進
有機合成化学協会誌 2008, 66, 124-138. DOI: 10.5059/yukigoseikyokaishi.66.124
2. Steocontrolled Synthesis of Functionalized Spirocyclic Compounds Based on Claisen Rearrangement and its Application to the Synthesis of Spirocyclic Sesquiterpenes and Pyrrolidinoindoline Alkaloids
Atsuo Nakazaki, Susumu Kobayashi
Synlett 2012, 1427-1455. DOI: 10.1055/s-0031-1290982
3. 軸性キラリティーを有するN-アリールオキシインドール誘導体を利用した不斉合成法の開発
中崎敦夫
有機合成化学協会誌 2017, 75, 821-830. DOI: 10.5059/yukigoseikyokaishi.75.821
著書
1. Debromoflustramine B
小林進、中崎敦夫
天然物の全合成 2000~2008 (日本), P. 48（有機合成化学協会編, 化学同人, 2009）.
2. カスケード型環化反応による環状グアニジン天然物の合成
西川俊夫、中崎敦夫
CSJカレントレビュー第29号 天然物の全合成, P. 86-93（日本化学会編, 化学同人, 2017）.
解説
1. 不斉有機分子触媒の新しい活性化法 －“SOMO 活性化”を活用したカスケード反応
西川俊夫、中崎敦夫
月刊化学 2010, 65, 68-69.