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Efficient synthesis of 13C-labelled erythromycin biosynthetic intermediate. 1: S-2-acetylaminoethyl (2 R,3 R,4 R,5 R)-3,5-diacetoxy-2,4-dimethyl-4-([13C]methoxy)-heptanethioate.
Published in:
Journal of Labelled Compounds & Radiopharmaceuticals, 2008, v. 51, n. 5, p. 213, doi. 10.1002/jlcr.1507
By:
- Iida, Katsumi;
- Kajiwara, Masahiro;
- Inoue-Tanihata, Tomoko;
- Fukui, Mineo;
- Nakata, Tadashi;
- Oishi, Takeshi
Publication type:
Article
Efficient syntheses of 13C-labelled erythromycin biosynthetic intermediates. 2: (2 S,3 S,4 S,5 R,6 R,7 R)-3,6,7-trihydroxy-2,4,6-trimethyl[1-13C]nonan-5-olide and S-2-acetylaminoethyl (2 R,3 S,4 S,5 R,6 S,7 R)-3,5,6,7-tetrahydroxy-2,4,6-trimethyl[1-13C]nonanethioate
Published in:
Journal of Labelled Compounds & Radiopharmaceuticals, 2008, v. 51, n. 5, p. 218, doi. 10.1002/jlcr.1506
By:
- Iida, Katsumi;
- Kajiwara, Masahiro;
- Fukui, Mineo;
- Nakata, Tadashi;
- Oishi, Takeshi
Publication type:
Article
Biological Sciences: New Type of Compound with Strong Sweetness.
Published in:
Nature, 1971, v. 233, n. 5322, p. 619, doi. 10.1038/233619a0
By:
- TAHARA, AKIRA;
- NAKATA, TADASHI;
- OHTSUKA, YASUO
Publication type:
Article
SmI2-induced cyclizations and their applications in natural product synthesis.
Published in:
Chemical Record, 2010, v. 10, n. 3, p. 159, doi. 10.1002/tcr.200900027
By:
- Nakata, Tadashi
Publication type:
Article
Biomimetic Oxidation of Aldehyde with NAD+ Models: Glycolysis-Type Hydrogen Transfer in an NAD+/NADH Model System.
Published in:
Angewandte Chemie International Edition, 1998, v. 37, n. 10, p. 1410, doi. 10.1002/(SICI)1521-3773(19980605)37:10<1410::AID-ANIE1410>3.0.CO;2-G
By:
- Kanomata, Nobuhiro;
- Suzuki, Masayuki;
- Yoshida, Mamiko;
- Nakata, Tadashi
Publication type:
Article
Highly Enantioselective Reduction with Novel, Bridged NADH Models.
Published in:
Angewandte Chemie International Edition, 1997, v. 36, n. 11, p. 1207, doi. 10.1002/anie.199712071
By:
- Kanomata, Nobuhiro;
- Nakata, Tadashi
Publication type:
Article
Total Synthesis of (+)-Batzelladine A and (−)-Batzelladine D, and Identification of Their Target Protein.
Published in:
Chemistry - A European Journal, 2005, v. 11, n. 23, p. 6878, doi. 10.1002/chem.200500852
By:
- Jun Shimokawa;
- Takanori Ishiwata;
- Koji Shirai;
- Hiroyuki Koshino;
- Aya Tanatani;
- Tadashi Nakata;
- Yuichi Hashimoto;
- Kazuo Nagasawa
Publication type:
Article
Stereoselective Total Synthesis of Mucocin, an Antitumor Agent.
Published in:
Angewandte Chemie International Edition, 2002, v. 41, n. 24, p. 4751, doi. 10.1002/anie.200290038
By:
- Takahashi, Shunya;
- Kubota, Akemi;
- Nakata, Tadashi
Publication type:
Article
C
Published in:
Angewandte Chemie International Edition, 2002, v. 41, n. 15, p. 2832, doi. 10.1002/1521-3773(20020802)41:15<2832::AID-ANIE2832>3.0.CO;2-Q
By:
- Kita, Tetsuya;
- Georgieva, Angelina;
- Hashimoto, Yuichi;
- Nakata, Tadashi;
- Nagasawa, Kazuo
Publication type:
Article

Found: 9

Efficient synthesis of <sup>13</sup>C-labelled erythromycin biosynthetic intermediate. 1: S-2-acetylaminoethyl (2 R,3 R,4 R,5 R)-3,5-diacetoxy-2,4-dimethyl-4-([<sup>13</sup>C]methoxy)-heptanethioate.

Efficient syntheses of <sup>13</sup>C-labelled erythromycin biosynthetic intermediates. 2: (2 S,3 S,4 S,5 R,6 R,7 R)-3,6,7-trihydroxy-2,4,6-trimethyl[1-<sup>13</sup>C]nonan-5-olide and S-2-acetylaminoethyl (2 R,3 S,4 S,5 R,6 S,7 R)-3,5,6,7-tetrahydroxy-2,4,6-trimethyl[1-<sup>13</sup>C]nonanethioate

Biological Sciences: New Type of Compound with Strong Sweetness.

SmI<sub>2</sub>-induced cyclizations and their applications in natural product synthesis.

Biomimetic Oxidation of Aldehyde with NAD<sup>+</sup> Models: Glycolysis-Type Hydrogen Transfer in an NAD<sup>+</sup>/NADH Model System.

Highly Enantioselective Reduction with Novel, Bridged NADH Models.

Total Synthesis of (+)-Batzelladine A and (−)-Batzelladine D, and Identification of Their Target Protein.

Stereoselective Total Synthesis of Mucocin, an Antitumor Agent.

C