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Organic Letters
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September 27, 2002
Synthesis of the hydroazulene portion of guanacastepene A from the cyclopentannelation reaction
Atsuo Nakazaki, Utpal Sharma, Marcus A Tius
ACS Omega
|
August 29, 2019
Palladium-Catalyzed Cascade Wacker/Allylation Sequence with Allylic Alcohols Leading to Allylated Dihydropyrones
Wen-Yu Huang, Toshio Nishikawa, Atsuo Nakazaki
Organic Letters
|
January 26, 2017
Biomimetic Synthesis and Structural Revision of Chaxine B and Its Analogues
Yushi Hirata, Atsuo Nakazaki, Hirokazu Kawagishi, et al.
Free Radical Biology & Medicine
|
March 24, 2020
Quantitative analysis of oxidized vitamin B1 metabolites generated by hypochlorous acid
Hitoshi Sasatsuki, Atsuo Nakazaki, Koji Uchida, et al.
Chemistry, an Asian Journal
|
September 16, 2016
A Divergent Approach to the Diastereoselective Synthesis of 3,3-Disubstituted Oxindoles from Atropisomeric N-Aryl Oxindole Derivatives
Atsuo Nakazaki, Ayako Mori, Susumu Kobayashi, et al.
Chemical & Pharmaceutical Bulletin
|
March 4, 2008
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, et al.
Organic Letters
|
October 27, 2017
Synthetic Route to Oscillatoxin D and Its Analogues
Yoshihiko Nokura, Yusuke Araki, Atsuo Nakazaki, et al.
Organic Letters
|
February 19, 2009
A switch of facial selectivities using alpha-heteroatom-substituted aldehydes in the vinylogous Mukaiyama aldol reaction
Mariko Shinoyama, Shin-ichi Shirokawa, Atsuo Nakazaki, et al.
The Journal of Organic Chemistry
|
March 9, 2026
Asymmetric Total Synthesis of Both C14 Epimers of Petromyzestrosterol Enables Stereochemical Assignment and Olfactory Activity Evaluation in Sea Lamprey
Rio Terasawa, Anne M Scott, Weiming Li, et al.
Chemical & Pharmaceutical Bulletin
|
May 8, 2013
Deprotection of the methoxymethyl group on 3-spiro-2-oxindole under basic conditions
Atsuo Nakazaki, Kanako Iwakiri, Tomohiro Hirano, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 51) with videos related to
Sort By:
Page
of 6
Organic Letters
|
September 27, 2002
Synthesis of the hydroazulene portion of guanacastepene A from the cyclopentannelation reaction
Atsuo Nakazaki, Utpal Sharma, Marcus A Tius
ACS Omega
|
August 29, 2019
Palladium-Catalyzed Cascade Wacker/Allylation Sequence with Allylic Alcohols Leading to Allylated Dihydropyrones
Wen-Yu Huang, Toshio Nishikawa, Atsuo Nakazaki
Organic Letters
|
January 26, 2017
Biomimetic Synthesis and Structural Revision of Chaxine B and Its Analogues
Yushi Hirata, Atsuo Nakazaki, Hirokazu Kawagishi, et al.
Free Radical Biology & Medicine
|
March 24, 2020
Quantitative analysis of oxidized vitamin B1 metabolites generated by hypochlorous acid
Hitoshi Sasatsuki, Atsuo Nakazaki, Koji Uchida, et al.
Chemistry, an Asian Journal
|
September 16, 2016
A Divergent Approach to the Diastereoselective Synthesis of 3,3-Disubstituted Oxindoles from Atropisomeric N-Aryl Oxindole Derivatives
Atsuo Nakazaki, Ayako Mori, Susumu Kobayashi, et al.
Chemical & Pharmaceutical Bulletin
|
March 4, 2008
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, et al.
Organic Letters
|
October 27, 2017
Synthetic Route to Oscillatoxin D and Its Analogues
Yoshihiko Nokura, Yusuke Araki, Atsuo Nakazaki, et al.
Organic Letters
|
February 19, 2009
A switch of facial selectivities using alpha-heteroatom-substituted aldehydes in the vinylogous Mukaiyama aldol reaction
Mariko Shinoyama, Shin-ichi Shirokawa, Atsuo Nakazaki, et al.
The Journal of Organic Chemistry
|
March 9, 2026
Asymmetric Total Synthesis of Both C14 Epimers of Petromyzestrosterol Enables Stereochemical Assignment and Olfactory Activity Evaluation in Sea Lamprey
Rio Terasawa, Anne M Scott, Weiming Li, et al.
Chemical & Pharmaceutical Bulletin
|
May 8, 2013
Deprotection of the methoxymethyl group on 3-spiro-2-oxindole under basic conditions
Atsuo Nakazaki, Kanako Iwakiri, Tomohiro Hirano, et al.
Page
of 6