Syntheses of methylated catechins and theaflavins using 2-nitrobenzenesulfonyl group to protect and deactivate phenol (English)
- New search for: Asakawa, T.
- New search for: Kawabe, Y.
- New search for: Yoshida, A.
- New search for: Aihara, Y.
- New search for: Manabe, T.
- New search for: Hirose, Y.
- New search for: Sakurada, A.
- New search for: Inai, M.
- New search for: Hamashima, Y.
- New search for: Furuta, T.
- New search for: Asakawa, T.
- New search for: Kawabe, Y.
- New search for: Yoshida, A.
- New search for: Aihara, Y.
- New search for: Manabe, T.
- New search for: Hirose, Y.
- New search for: Sakurada, A.
- New search for: Inai, M.
- New search for: Hamashima, Y.
- New search for: Furuta, T.
In:
JOURNAL OF ANTIBIOTICS
;
69
, 4
;
299-312
;
2016
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ISSN:
- Article (Journal) / Print
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Title:Syntheses of methylated catechins and theaflavins using 2-nitrobenzenesulfonyl group to protect and deactivate phenol
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Contributors:Asakawa, T. ( author ) / Kawabe, Y. ( author ) / Yoshida, A. ( author ) / Aihara, Y. ( author ) / Manabe, T. ( author ) / Hirose, Y. ( author ) / Sakurada, A. ( author ) / Inai, M. ( author ) / Hamashima, Y. ( author ) / Furuta, T. ( author )
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Published in:JOURNAL OF ANTIBIOTICS ; 69, 4 ; 299-312
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Publisher:
- New search for: JAPAN ANTIBIOTICS RES ASSOC
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Publication date:2016-01-01
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Size:14 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 615.329
- Further information on Dewey Decimal Classification
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Classification:
DDC: 615.329 -
Source:
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Table of contents – Volume 69, Issue 4
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 189
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Amos B Smith, III: chemist, collaborator and mentorWood, John L et al. | 2016
- 190
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Professor Amos B Smith, IIISunazuka, Toshiaki et al. | 2016
- 191
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The first total synthesis and the second- or third-generation approachAjito, Keiichi et al. | 2016
- 192
-
Organic synthesis in the Smith Group: a personal selection of a dozen lessons learned at the University of PennsylvaniaMinbiole, Kevin P C et al. | 2016
- 203
-
Strategies for construction of the all-carbon macrocyclic skeleton of the ansamycin antibiotic-kendomycinXu, Shu et al. | 2016
- 213
-
The Petasis-Ferrier rearrangement: developments and applicationsMinbiole, Emily C et al. | 2016
- 220
-
Synthesis of the phorboxazoles-potent, architecturally novel marine natural productsShultz, Zachary et al. | 2016
- 253
-
Total syntheses of codonopsinine and 4-epi-codonopsinine via gold-mediated tandem-catalyzed pyrrole synthesisYamaguchi, Minami et al. | 2016
- 259
-
Synthesis of the ABCDEF and FGHI ring system of yessotoxin and adriatoxinZhang, Yuan et al. | 2016
- 273
-
Practical synthesis of the C-ring precursor of paclitaxel from 3-methoxytolueneFukaya, Keisuke et al. | 2016
- 280
-
Total synthesis of ent-(+)-cinanthrenol AZhu, Liangyu et al. | 2016
- 287
-
Synthesis and structure-activity relationship study of FD-891: importance of the side chain and C8-C9 epoxide for cytotoxic activity against cancer cellsItagaki, Tomohiro et al. | 2016
- 294
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Stereoselective access to tubuphenylalanine and tubuvaline: improved Mn-mediated radical additions and assembly of a tubulysin tetrapeptide analogFriestad, Gregory K et al. | 2016
- 299
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Syntheses of methylated catechins and theaflavins using 2-nitrobenzenesulfonyl group to protect and deactivate phenolAsakawa, Tomohiro et al. | 2016
- 313
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Proline-based phosphoramidite reagents for the reductive ligation of S-nitrosothiolsPark, Chung-Min et al. | 2016
- 319
-
Non-antibiotic 12-membered macrolides: design, synthesis and biological evaluation in a cigarette-smoking modelSugawara, Akihiro et al. | 2016
- 327
-
The use of fluorescently-tagged apoptolidins in cellular uptake and response studiesChong, Katherine M et al. | 2016
- 331
-
Synthetic studies toward citrinadin A: construction of the pentacyclic coreMcCallum, Monica E et al. | 2016
- 337
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The enantioselective synthesis and biological evaluation of chimeric promysalin analogs facilitated by diverted total synthesisKnouse, Kyle W et al. | 2016
- 340
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Furan-iminium cation cyclization (FIC) in a total synthesis of manzamine alkaloidsTokumaru, Kazuyuki et al. | 2016
- 344
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Natural product-derived quaternary ammonium compounds with potent antimicrobial activityJoyce, Maureen D et al. | 2016
- 348
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Anti-obesity activities of the yoshinone A and the related marine γ-pyrone compoundsKoyama, Tomoyuki et al. | 2016