D. Kaelin

发表

Structure activity relationship of N-1 substituted 1,5-naphthyrid-2-one analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-9).

Akinori Nishimura, P. Meinke, D. Olsen, 2022, Bioorganic & medicinal chemistry letters.

Catalytic Enantioselective Addition of Dialkylzincs to Aldehydes Using (2S)‐(−)‐3‐exo‐(Dimethylamino)Isoborneol [(2S)‐DAIB]: (S)‐1‐Phenyl‐1‐Propanol

S. Denmark, R. Noyori, S. Suga, 2003 .

Catalytic enantioselective addition of dialkylzincs to aldehydes using (2S)-(-)-3-exo-(dimethylamino)isoborneol [(2S)-daib]: (S)-1-phenyl-1-propanol: [Benzenemethanol, α-ethyl-, (S)-]

S. Denmark, R. Noyori, S. Suga, 2002 .

In Vitro and In Vivo Characterization of the Novel Oxabicyclooctane-Linked Bacterial Topoisomerase Inhibitor AM-8722, a Selective, Potent Inhibitor of Bacterial DNA Gyrase

Akinori Nishimura, Jin Wu, C. Garlisi, 2016, Antimicrobial Agents and Chemotherapy.

Novel methodologies for the synthesis of C-aryl glycosides and progress toward the synthesis of the C-aryl glycoside natural products galtamycinone and kidamycin

D. Kaelin, 2002 .

Total synthesis of (+)-ambruticin S.

M. Schneider, S. Martin, T. Kirkland, 2001, Journal of the American Chemical Society.

Total synthesis of isokidamycin.

S. Martin, Douglas Mans, D. Kaelin, 2010, Journal of the American Chemical Society.

Studies Toward the Syntheses of Pluramycin Natural Products. The First Total Synthesis of Isokidamycin.

S. Martin, Douglas Mans, D. Kaelin, 2011, Tetrahedron.

General entries to C-aryl glycosides. Formal synthesis of galtamycinone

Beth Apsel, S. Martin, O. Lopez, 2003 .

General strategies for the synthesis of the major classes of C-aryl glycosides.

S. Martin, O. Lopez, S. F. Martín, 2001, Journal of the American Chemical Society.

Structure activity relationship of C-2 ether substituted 1,5-naphthyridine analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-5).

Akinori Nishimura, Jin Wu, P. Meinke, 2015, Bioorganic & medicinal chemistry letters.

Tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of left-hand-side moiety (Part-2).

Leo A. Joyce, E. Sherer, R. Nargund, 2015, Bioorganic & medicinal chemistry letters.

Oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad spectrum antibacterial agents.

Sangita Patel, Jin Wu, P. Meinke, 2014, ACS medicinal chemistry letters.

C1–C2-linker substituted 1,5-naphthyridine analogues of oxabicyclooctane-linked NBTIs as broad-spectrum antibacterial agents (part 7)

Akinori Nishimura, Jin Wu, Xuanjia Peng, 2015 .

Structure activity relationship of pyridoxazinone substituted RHS analogs of oxabicyclooctane-linked 1,5-naphthyridinyl novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-6).

Akinori Nishimura, Jin Wu, Xuanjia Peng, 2015, Bioorganic & medicinal chemistry letters.

Regioselective synthesis of unsymmetrical C-aryl glycosides using silicon tethers as disposable linkers.

S. M. Sparks, S. Martin, D. Kaelin, 2003, Journal of the American Chemical Society.

Regioselective Synthesis of Unsymmetrical C‐Aryl Glycosides Using Silicon Tethers as Disposable Linkers.

S. M. Sparks, S. Martin, D. Kaelin, 2004 .

4-arylcyclohexylalanine analogs as potent, selective, and orally active inhibitors of dipeptidyl peptidase IV.

Joseph L Duffy, G. Scapin, N. Thornberry, 2007, Bioorganic & medicinal chemistry letters.