佐藤研究室 慶應義塾大学理工学部応用化学科      English

原著論文

67. Lactam Strategy Using Amide-Selective Nucleophilic Addition for the Quick Access to Complex Amines: Unified Total Synthesis of Stemoamide-Type Alkaloids

Sugiyama, Y.; Soda, Y.; Yoritate, M.; Tajima, H.; Takahashi, Y.; Shibuya, K.; Ogihara, C.; Yokoyama, T.; Oishi, T.; *Sato, T.; *Chida, N.
Bull. Chem. Soc. Jpn. 2022, 95, 278–287.

This article was selected as the Selected Paper.
This article was selected as the inside cover.


66. Total Synthesis of Paclitaxel

Iiyama, S.; Fukaya, K.; Yamaguchi, Y.; Watanabe, A.; Yamamoto, H.; Mochizuki, S.; Saio, R.; Noguchi, T.; Oishi, T.; Sato, T.; *Chida, N.
Org. Lett. 2022, 24, 202–206.

This article was selected as the most read articles on a monthly basis.
This article was selected as the most read articles on an annual basis.


65. Crystal structure of (+)-(1S,5S,6S,7S,10S,11S,16S)-16-hydroxy-7-(methoxymethoxy)- 11,15,18,18-tetramethyl-3,13-dioxo-2,4-dioxatetracyclo[12.3.1.01,5.06,11]octadec-14-en-10-yl benzoate

*Oishi, T.; Fukaya, K.; Sato, T.; Chida, N.
Acta Cryst. 2021, E77, 1234–1238.


64. Development of Chiral N-Alkoxyamide Strategy and Application to Asymmetric Total Synthesis of Fasicularin

Minamikawa, R.; Fukaya, K.; Kobayashi, A.; Komiya, Y.; Yamamoto, S.; Urabe, D.; Chida, N.; *Sato, T.
Synthesis 2021, 53, 4621–4635.

This Feature Article was invited.


63. Five-Step Total Synthesis of (±)-Aspidospermidine by a Lactam Strategy via an Azomethine Ylide

Katahara, S.; Sugiyama, Y.; Yamane, M.; Komiya, Y.; *Sato, T.; *Chida, N.
Org. Lett. 2021, 23, 3058–3063.

This article was selected as the most read articles on a monthly basis.


62. Seven-step Synthesis of All-nitrogenated Sugar Derivatives Using Sequential Overman Rearrangements

Okuyama, Y.; Kidena, M.; Kato, E.; Kawano, S.; Ishii, K.; Maie, K.; Miura, K.; Simizu, S.; *Sato, T.; *Chida, N.
Angew. Chem. Int. Ed. 2021, 60, 5193–5198.

This article was selected as a Hot Paper.
This article was selected as an inside back cover.


61. Identification of madangamine A as a novel lysosomotropic agent to inhibit autophagy

Miura, K.; Kawano, S.; Suto, T.; Sato, T.; Chida, N.; *Simizu S.
Bioorg. Med. Chem. 2021, 34, 116041.

This article was selected as a front cover.


60. Synthesis of Saxitoxin and Its Derivatives

Okuyama, Y.; Okamoto, R.; Mukai, Kinoshita, K.; Sato, T.; *Chida, N.
Org. Lett. 2020, 22, 8697–8701.


59. Unified Total Synthesis of Pentacyclic Stemoamide-type Alkaloids

Soda, Y.; Sugiyama, Y.; Yoritate, M.; Tajima, H.; Shibuya, K.; Ogihara, C.; Oishi, T.; *Sato, T., *Chida, N.
Org. Lett. 2020, 22, 7502–7507.

This article was selected as the most read articles on a monthly basis.
This article was selected as the most read articles on an annual basis.


58. Copper-Catalyzed Electrophilic Etherification of Arylboronic Esters with Isoxazolidines

Katahara, S,; Takahashi, T.; Nomura, K.; *Uchiyama, M.; *Sato, T.; *Chida, N.
Chem. Asian J. 2020, 15, 1869–1872.

This article was selected as an VIP paper.


57. Enantioselective Stereodivergent Approach to α-Hydroxy Skipped Dienes: Synthesis of the Western Polyene Fragment of Corallopyronin A

Nagashima, Y.; Okada, Y.; *Sato, T.; *Chida, N.
Chem. Lett. 2019, 48, 1519–1521.


56. Iridium-Catalyzed Reductive Nucleophilic Addition to Tertiary Amides

Takahashi, Y.; Yoshii, R.; *Sato, T.; *Chida, N.
Chem. Lett. 2019, 48, 1138–1141.

This article was selected as an Editor’s Choice.


55. Copper-Catalyzed Electrophilic Amidation of Organotrifluoroborates with Use of N-Methoxyamides

Banjo, S.; B.; Nakasuji, E.; Meguro, T.; *Sato, T.; *Chida, N.
Chem. Eur. J. 2019, 25, 7941–7947.


54. Total Synthesis of (–)-Zephyranthine

Ishii, K.; Seki-Yoritate, Y.; Ishibashi, M.; Liaw, M. W.; Oishi, T.; *Sato, T.; *Chida, N.
Heterocycles 2019, 99, 111–117.

This article was invited as a special issue in honor of Professor Tohru Fukuyama on 70th Birthday.


53. Nucleophilic Approach to Fully Substituted Cyclic Nitrones from N-Hydroxylactam Derivatives: Development and Application to the Total Synthesis of Cylindricine C

Hiraoka, S.; Matsumoto, T.; Matsuzaka, K.; *Sato, T.; *Chida, N.
Angew. Chem. Int. Ed. 2019, 58, 4381–4385.

This article was selected as a Hot Paper.


52. Asymmetric Total Synthesis of Fasicularin by Chiral N-Alkoxyamide Strategy

Yamamoto, S.; Komiya, Y.; Kobayashi, A.; Minamikawa, R.; Oishi, T.; *Sato, T.; *Chida, N.
Org. Lett. 2019, 21, 1868–1871.


51. Unified Total Synthesis of Madangamine Alkaloids

Suto, T.; Yanagita, Y.; Nagashima, Y.; Takikawa, S.; Kurosu, Y.; Matsuo, N.; Miura, K.; Simizu, S.; *Sato, T.; *Chida, N.
Bull. Chem. Soc. Jpn. 2019, 92, 545–571.

This article was selected as Top Accessed Articles.
This article was selected as the Selected Paper.


50. Iridium-Catalyzed Reductive Nucleophilic Addition to Secondary Amides

Takahashi, Y.; Yoshii, R.; *Sato, T.; *Chida, N.
Org. Lett. 2018, 20, 5705–5708.


49. Crystal structure of (–)-(R,E)-3-(1,3-benzodioxol-5-yl)-5-[(4S,5R)-5-hydroxymethyl-2,2-dimethyl-1,3-dioxolan-4-yl]-N,N-dimethylpent-4-enamide

*Oishi, T.; Ishii, K.; Ishibashi, M.; Sato T.; Chida, N.
Acta Cryst. 2018, E74, 825–828.


48. Crystal structure of (−)-(5R,7R,8S,9R,10S )-8-methyl-7-[(5R )- 3-methyl-2-oxooxolan-3-en-5-yl]-1-aza-6-oxatricyclo-[8.3.0.05,9]tridecan-13-one monohydrate

*Oishi, T.; Yoritate, M.; Sato T.; Chida, N.
Acta Cryst. 2018, E74, 555–558.


47. Stereodivergent Hydroboration of Allenes

Nagashima, Y.; Sasaki, K.; Suto, T.; *Sato, T.; *Chida, N.
Chem. Asian J. 2018, 13, 1024–1028.


46. Synthesis of Kaitocephalin Facilitated by Three Stereoselective Allylic Transposition Reactions

Sugai, T.; Okuyama, Y.; Shin, J.; Usui, S.; Hisada, S.; Osanai, R.; Oishi, T.; *Sato, T.; *Chida, N.
Chem. Lett. 2018, 47, 454–457.


45. Synthesis of β-Hydroxy-α,α-disubstituted Amino Acids through the Orthoamide-Type Overman Rearrangement of an α,β--Unsaturated Ester and Stereodivergent Intramolecular SN2’ Reaction: Development and Application to the Total Synthesis of Sphingofungin F

Sugai, T.; Usui, S.; Tsuzaki, S.; Oishi, H.; Yasushima, D.; Hisada, S.; Fukuyasu, T.; Oishi, T.; *Sato, T.; *Chida, N.
Bull. Chem. Soc. Jpn. 2018, 91, 594–607.

This article was selected as the Selected Paper.


44. Unified Total Synthesis of Stemoamide-Type Alkaloids by Chemoselective Assembly of Five-Membered Building Blocks

Yoritate, M.; Takahashi, Y.; Tajima, H.; Ogihara, C.; Yokoyama, T.; Soda, Y.; Oishi, T.; *Sato, T.; *Chida, N.
J. Am. Chem. Soc. 2017, 139, 18386‒18391.

This article was selected as the most read articles on a monthly basis.
This article was highlighted in SYNFACTS (2018, 14, 231).


43. Reductive Approach to Nitrones from N-Siloxyamides and N-Hydroxyamides

Katahara, S.; Kobayashi, S.; Fujita, K.; Matsumoto, T.; *Sato T.; *Chida, N.
Bull. Chem. Soc. Jpn. 2017, 90, 893‒904.

This article was selected as BCSJ award.
This article was selected as a front cover.


42. Crystal structure of (–)-methyl (R,E)-4-[(2R,4R )-2-amino-2-trichloromethyl-1,3-dioxolan-4-yl]-4-hydroxy-2-methylbut-2-enoate

*Oishi, T.; Kidena. M.; Sugai, T. Sato T.; Chida, N.
Acta Cryst. 2017, E73, 983–986.


41. Unified Total Synthesis of Madangamines A, C, and E

Suto, T.; Yanagita, Y.; Nagashima, Y.; Takikawa, S.; Kurosu, Y.; Matsuo, N.; *Sato T.; *Chida, N.
J. Am. Chem. Soc. 2017, 139, 2952‒2955.

This article was selected as the most read articles on a monthly basis.
This article was highlighted in SYNFACTS (2017, 13, 450).


40. Copper-Catalyzed Electrophilic Amination Using N-Methoxyamines

Fukami, Y.; Wada, T.; Meguro, T.; Chida, N.; *Sato, T.
Org. Biomol. Chem. 2016, 14, 5486‒5489.

This article was invited in New Talent Themed Issue.
This article was selected as a HOT article.


39. Crystal structure of (+)-N-[(1R,5S,6S,9S)-5-hydroxymethyl- 3,3,9-trimethyl-8-oxo-2,4,7-trioxabicyclo[4.3.0]nonan-9-yl]acetamide

*Oishi, T.; Tsuzaki, S.; Sugai, T. Sato T.; Chida, N.
Acta Cryst. 2016, E72, 756–759.


38. Total Synthesis of (–)-Stemoamide by Sequential Overman/Claisen Rearrangement

Nakayama, Y.; Maeda, Y.; Hama, N.; *Sato T.; *Chida, N.
Synthesis, 2016, 48, 1647‒1654.

This article was invited in Target Oriented Synthesis of Complex Molecules Issue.


37. Crystal structure of (+)-methyl (E)-3-[(2S,4S,5R)-2-amino-5-hydroxymethyl-2-trichloromethyl-1,3-dioxolan-4-yl]-2-methylprop-2-enoate

*Oishi, T.; Yasushima, D.; Yuasa, K.; Sato T.; Chida, N.
Acta Cryst. 2016, E72, 343–346.


36. Practical Synthesis of the C-ring Precursor of Paclitaxel from 3-Methoxytoluene

Fukaya, K.; Yamaguchi, Y.; Watanabe, A.; Yamamoto, H.; Sugai, S.; Sugai, T.; Sato T.; *Chida, N.
J. Antibiot. 2016, 69, 273‒279.

35. An Iridium-Catalyzed Reductive Approach to Nitrones from N-Hydroxyamides

Katahara, S.; Kobayashi, S.; Fujita, K.; Matsumoto, T.; *Sato T.; *Chida, N.
J. Am. Chem. Soc. 2016, 138, 5246‒5249.


34. Enantioselective Total Synthesis of (+)-Neostenine

Nakayama, Y.; Maeda, Y.; Kotatsu, M.; Sekiya, R.; Ichiki, M.; *Sato, T.; *Chida, N.
Chem. Eur. J. 2016, 22, 3300‒3303.


33. Synthesis of (±)-Lasubine II Using N-Methoxyamines

Yokoyama, T.; Fukami, Y.; *Sato, T.; *Chida, N.
Chem. Asian J. 2016, 11, 470‒473.


32. Crystal structure of (±)-(5SR,6SR )-6-ethenyl-1-[(RS)-1-phenylethoxy]-1-azaspiro[4.5]decan-2-one

*Oishi, T.; Yamamoto, S.; Yokoyama, T.; Kobayashi, A.; Sato T.; Chida, N.
Acta. Cryst. 2015, E71, 1528‒1530.


31. Crystal structure of (±)-(7RS,8SR)-7-methyl-1,4-dioxaspiro[4.5]decane-7,8-diol

*Oishi, T.; Yamamoto, H.; Sugai, T.; Fukaya, K.; Yamaguchi, Y.; Watanabe, A.; Sato T.; Chida, N.
Acta. Cryst. 2015, E71, 1181‒1184.


30. Synthesis of Paclitaxel. 2. Construction of the ABCD-Ring and Formal Synthesis

Fukaya, K.; Kodama, K.; Tanaka, Y.; Yamazaki, H.; Sugai, T.; Yamaguchi, Y.; Watanabe, A.; Oishi, T.; *Sato, T.; *Chida, N.
Org. Lett. 2015, 17, 2574‒2577.


29. Synthesis of Paclitaxel. 1. Synthesis of the ABC-Ring of Paclitaxel by SmI2-Mediated Cyclization

Fukaya, K.; Tanaka, Y.; Sato, A.; Kodama, K.; Yamazaki, H.; Ishimoto, T.; Nozaki, Y.; Iwaki, Y.; Yuki, Y.; Umei, K.; Sugai, T.; Yamaguchi, Y.; Watanabe, A.; Oishi, T.; Sato, T.; *Chida, N.
Org. Lett. 2015, 17, 2570‒2573.

This article was selected as the most read articles on a monthly basis.


28. Crystal structure of (±)-(1SR,5SR,6SR,7SR,10SR,11SR,13SR)-13-benzyloxy-7-methoxymethoxy-11,15,18,18-tetramethyl-3-oxo-2,4-dioxatetracyclo[12.3.1.01,5.06,11]octadeca-14,16-dien-10-ylbenzoate

*Oishi, T.; Fukaya, K.; Yamaguchi, Y.; Sugai, T., Watanabe, A.; Sato T.; Chida N.
Acta. Cryst. 2015, E71, 490‒493.


27. Crystal structures of (±)-(1SR,5SR,6SR,7SR,10SR,11SR,13RS,14SR)-13-hydroxy-7-methoxymethoxy-11,15,18,18-tetramethyl-3-oxo-2,4-dioxatetracyclo[12.3.1.01,5.06,11]octadec-15-en-10-yl benzoate, its 13-epimer and 13-one derivative

*Oishi, T.; Fukaya, K.; Yamaguchi, Y.; Sugai, T., Watanabe, A.; Sato T.; Chida N.
Acta. Cryst. 2015, E71, 466‒472.


26. Synthesis of Diazatricyclic Common Structure of Madangamine Alkaloids

Yanagita, Y.; Suto, T.; Matsuo, N.; Kurosu, Y.; *Sato T.; *Chida, N.
Org. Lett. 2015, 17, 1946‒1949.


25. Total Synthesis of Sphingofungin F by Orthoamide-Type Overman Rearrangement of an Unsaturated Ester

Tsuzaki, S.; Usui, S.; Oishi, H.; Yasushima, D.; Fukuyasu, T.; Oishi, T.; *Sato T.; *Chida, N.
Org. Lett. 2015, 17, 1704‒1707.


24. Iridium-Catalyzed Chemoselective Reductive Nucleophilic Addition to N-Methoxyamides

Nakajima, M.; *Sato T.; *Chida, N.
Org. Lett. 2015, 17, 1696‒1699.


23. Total Syntheses of (±)-Gephyrotoxin and (±)-Perhydrogephyrotoxin

Shirokane, K.; Tanaka, Y.; Yoritate, M.; Takayama, N.; *Sato T.; *Chida, N.
Bull. Chem. Soc. Jpn. 2015, 88, 522‒537.

This article was selected as BCSJ award.
This article was selected as a front cover.


22. Crystal structure of (±)-(4RS,5RS,7SR)-4-[(1RS,2RS,3RS,6RS)-3-benzoyloxy-2-(2-hydroxyethyl)-6-methoxymethoxy-2-methylcyclohexyl]-8,10,10-trimethyl-2-oxo-1,3-dioxaspiro[4.5]dec-8-en-7-yl benzoate benzene monosolvate

*Oishi, T.; Yamaguchi, Y.; Fukaya, K.; Sugai, T., Watanabe, A.; Sato T.; Chida N.
Acta. Cryst. 2015, E71, 8‒11.


21. Chemoselective Reductive Nucleophilic Addition to Tertiary Amides, Secondary Amides and N-Methoxyamides

Nakajima, M.; Oda, Y.; Wada, T.; Minamikawa, R.; Shirokane, K.; *Sato, T.; *Chida, N.
Chem. Eur. J. 2014, 20, 17565‒17571.


20. (5R*)-5-[(2S*,5S*)-1-Methoxy-5-phenylpyrrolidin-2-yl]- 3-methylfuran-2(5H)-one

*Oishi, T.; Yoritate, M.; Sato, T.; Chida, N.
Acta Cryst. 2014, E70, o839.


19. Two-step Synthesis of Multi-Substituted Amines by Using an N-Methoxy Group as a Reactivity Control Element

Yoritate, M.; Meguro, T.; Matsuo, N.; Shirokane, K.; *Sato, T.; *Chida, N.
Chem. Eur. J. 2014, 20, 8210‒8216.

This article was selected as VIP (Very Important Paper).
This article was selected as a front cover.


18. Total Synthesis of (±)-Gephyrotoxin by Amide-Selective Reductive Nucleophilic Addition

Shirokane, K.; Wada, T.; Yoritate, M.; Minamikawa, R.; Takayama, N.; *Sato T.; *Chida, N.
Angew. Chem. Int. Ed. 2014, 53, 512‒516.

This article was selected as VIP (Very Important Paper).
This article was selected as the most accessed articles in 12/2013.
This article was selected as the most accessed articles in 11/2013-10/2014.
This article was highlighted in SYNFACTS (2014, 10, 116).


17. Cascade- and Orthoamide-type Overman Rearrangements of Allylic Vicinal Diols

Nakayama, Y.; Sekiya, R.; Oishi, H.; Hama, N.; Yamazaki, M.; *Sato, T.; *Chida, N.
Chem. Eur. J. 2013, 19, 12052‒12058.


16. Direct Nucleophilic Addition to N-Alkoxyamides

Yanagita, Y.; Nakamura, H.; Shirokane, K.; Kurosaki, Y.; *Sato, T.; *Chida, N.
Chem. Eur. J. 2013, 19, 678‒684.


15. Synthesis of (‒)-Morphine: Application of Sequential Claisen/Claisen Rearrangement of an Allylic Vicinal Diol

Ichiki, M.; Tanimoto, H.; Miwa, S.; Saito, R.; Sato, T.; *Chida, N.
Chem. Eur. J. 2013, 19, 264‒269.

This article was selected as the most read article Top 25 on an annually basis.


14. (+)-(1S,5R,6R)-6-[(S)-1-Hy­dr­oxy-2-(meth­­oxy­meth­yl­oxy)eth­yl]-1-methyl-3-tri­chloro­methyl-2-aza-4,7-dioxa­bi­cyclo­[3.3.0]oct-2-en-8-one

*Oishi, T.; Oishi, H.; Tsuzaki, S.; Sato, T.; Chida, N.
Acta Cryst. 2012, E68, o3185.


13. Chirality Transfers through Sequential Sigmatropic Rearrangements of Allylic Vicinal Diols: Development and Application to Total Synthesis of (–)-Kainic Acid

Kitamoto, K.; Nakayama, Y.; Sampei, M.; Ichiki, M.; Furuya, N.; *Sato, T.; *Chida, N.
Eur. J. Org. Chem. 2012, 4217‒4231.


12. Concise Synthesis of α-Trisubstituted Amines from Ketones Using N-Methoxyamines”

Kurosaki, Y.; Shirokane, K.; Oishi, T.; *Sato, T.; *Chida, N.
Org. Lett. 2012, 14, 2098‒2101.


11. Direct Chemoselective Allylation of Inert Amide Carbonyls

Oda, Y.; *Sato, T.; *Chida, N.
Org. Lett. 2012, 14, 950‒953.

This article was highlighted in SYNFACTS (2012, 14, 428).


10. Total Synthesis of Broussonetine F: The Orthoamide Overman Rearrangement of an Allylic Diol

Hama, N.; Aoki, T.; Miwa, S.; Yamazaki, M.; Sato, T.; *Chida, N.
Org. Lett. 2011, 13, 616‒619.

This article was selected as the most read articles on a monthly basis.
This article was selected as the most read articles for quarter 1, 2011.


9. Total Synthesis of (‒)-Salinosporamide A

Kaiya, Y.; Hasegawa, J.; Momose, T.; *Sato, T.; *Chida, N.
Chem. Asian J. 2011, 5, 209‒219.

This article was selected as the most read article Top 25 on an annually basis.


7. A Direct Entry to Substituted N-Methoxyamines from N-Methoxyamides via N-Oxyiminium Ions

Shirokane, K.; Kurosaki, Y.; *Sato, T.; *Chida, N.
Angew. Chem. Int. Ed. 2010, 49, 6369‒6372.

This article was highlighted in SYNFACTS (2010, 12, 1412).


6. Formal Synthesis of Salinosporamide A Starting from D-Glucose

Momose, T.; Kaiya, Y.; Hasegawa, J.; Sato, T.; *Chida, N.
Synthesis, 2009, 2983‒2991.


5. Total Synthesis of (‒)-Agelastatin A: The Application of a Sequential Sigmatropic Rearrangement

Hama, N.; Matsuda, T.; Sato, T.; *Chida, N.
Org. Lett. 2009, 11, 2687‒2690.

This article was highlighted in SYNFACTS (2009, 12, 1314).


4. Construction of Epidithiodioxopiperazines by Directed Oxidation of Hydroxyproline-Derived Dioxopiperazines

*Overman, L. E.; Sato, T.
Org. Lett. 2007, 9, 5267‒5270.

3. Total Synthesis and Bioactivity of an Unnatural Enantiomer of Merrilactone A: Development of an Enantioselective Desymmetrization Strategy

*Inoue, M.; Lee, N.; Kasuya, S.; Sato, T.; Hirama, M.; Moriyama, M.; Fukuyama, Y.
J. Org. Chem. 2007, 72, 3065–3075.

2. Asymmetric Total Synthesis of (‒)-Merrilactone A: Use of a Bulky Protecting Group as Long-Range Stereocontrolling Element

*Inoue, M.; Sato, T.; Hirama, M.
Angew. Chem. Int. Ed. 2006, 45, 4843–4848.

1. Total Synthesis of Merrilactone A

*Inoue, M.; Sato, T.; Hirama, M.
J. Am. Chem. Soc. 2003, 125, 10772–10773.


総説

7. 立体発散的スキップジエン合成法の開発とマダンガミン類の網羅的全合成

*佐藤隆章
有機合成化学協会誌 2022, 80, 343–356.

有機合成化学奨励賞 受賞論文


6. Total Synthesis of Skipped Diene Natural Products

*Sato, T.; Suto, T. Nagashima, Y.; Mukai S. Chida, N.
Asian J. Org. Chem. 2021, 10, 2486–2502.

This is an invited review.


5. Total Synthesis of Complex Alkaloids by Nucleophilic Addition to Amides

*Sato, T.; Yoritate, M.; Tajima, H.; Chida, N.
Org. Biomol. Chem. 2018, 16, 3864–3875.

This is an invited review.


4. N-アルコキシアミド基への求核付加反応の開発とゲフィロトキシンの全合成

佐藤隆章、千田憲孝
有機合成化学協会誌 2016, 74, 599–610.


3. Synthesis of Natural Products Containing Cyclohexane Units Utilizing the Ferrier Carbocyclization Reaction

*Chida, N.; Sato, T.
Chem. Rec. 2014, 14, 592–605.


2. Nucleophilic Addition to N-Alkoxyamides

*Sato, T.; Chida, N.
Org. Biomol. Chem. 2014, 12, 3147–3150.

This is an invited account.
This article was selected as one of the highly cited articles.


1. メリラクトンAの全合成:遠隔不斉誘導と不斉非対称化

井上将行, 佐藤隆章, 平間正博
有機合成化学協会誌 2007, 65, 419–429.


著書

3. Chiral Pool Synthesis: Chiral Pool Syntheses Starting from Carbohydrates

Chida, N.; Sato, T.
Comprehensive Chirality, Carreira, E. M.; Yamamoto, H.; Elsevier Science, 2012, pp. 207‒239.

2. [2+2]光付加環化

井上将行, 佐藤隆章
天然物合成で活躍した反応 実験のコツとポイント, 有機合成化学協会編, 化学同人, 2011, pp. 62‒63.

1. 対称性を利用したメリラクトンAの全合成 遠隔不斉誘導と不斉非対称化

井上将行, 佐藤隆章, 平間正博
天然物全合成の最新動向, 監修 北泰行, シーエムシー出版, 2009, pp. 3‒17.


解説・その他

7. 博士進学? 研究室の学生に聞いてみた?

佐藤隆章
化学と工業 2021, 74, 30–31.(転載許可済)


6. 天然物合成で総収率を上げるには?

佐藤隆章
有機合成化学協会誌 2018, 76, 454–457.


5. アミド基選択的な求核付加反応の開発と応用

佐藤隆章
化学と工業, 2017, 70, 621–622.

4. アミド基選択的な求核付加反応による天然物全合成の効率化

佐藤隆章
化学と工業, 2014, 67, 786.

3. Cover Profile: Two-step Synthesis of Multi-substituted Amines Using N-Methoxy Group as a Reactivity Control Element

Yoritate, M.; Meguro, T.; Matsuo, N.; Shirokane, K.; *Sato, T.; *Chida, N.
Chem. Eur. J. 2014, 20, 7849.

2. カチオン-π相互作用を利用した有機合成化学

千田憲孝、佐藤隆章
化学, 2008, 63, 66-67.

1. 酸化的カップリング反応を用いたインドールアルカロイド類の全合成

佐藤隆章
有機合成化学協会誌, 2006, 64, 679–670.