Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Jenny M. Baxter"'
Autor:
Jenny M. Baxter, Maria Teresa Diez, Fernando Pelaez, Craig A. Parish, Kenneth E. Wilson, Samantha Tucker-Samaras, Scott K. Smith, Mercedes de la Cruz, Javier Collado, Deborah L. Zink, Gonzalo Platas, Francisca Vicente, Gerald F. Bills
Publikováno v:
Journal of Natural Products. 72:59-62
Antisense-based screening strategies can be used to sensitize a microorganism and selectively detect inhibitors against a particular cellular target of interest. A strain of Staphylococcus aureus that generates an antisense RNA against SecA, a centra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10adf7768949be995677f32dadb3aac9
https://doi.org/10.1021/np800528a
https://doi.org/10.1021/np800528a
Autor:
Ian W. Davies, Michael Palucki, Eugenia Njolito, Jason J. Kowal, Wenjie Li, Jonathan D. Rosen, Jenny M. Baxter, Jacob M. Janey, Rick Sidler, Orella Charles J
Publikováno v:
The Journal of Organic Chemistry. 73:3212-3217
An expedient, five step synthesis of caprolactam 1 is reported starting from natural L-homoserine. The key step is a chemoselective reductive cyclization of alpha,beta-unsaturated nitrile 10 mediated by Raney-Co type metals. This hydrogenation is ext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41dcfc5d49e24b2d724c04e750c9f38e
https://doi.org/10.1021/jo8000996
https://doi.org/10.1021/jo8000996
Autor:
Kevin M. Belyk, Ian W. Davies, Shane W. Krska, Dietrich Steinhuebel, Brian C. Bishop, Jenny M. Baxter, Anthony Alorati, Michael Palucki, Yongkui Sun
Publikováno v:
Organic Letters. 12:4201-4203
A general method for the enantioselective hydrogenation of protected allylic amine derivatives is described. This procedure relies on the generation of a cationic ruthenium complex with the axially chiral ligand (-)-TMBTP. The utility is highlighted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d100972aef7682bf747e36ede25adfa4
https://doi.org/10.1021/ol101804e
https://doi.org/10.1021/ol101804e
Autor:
Gonzalo Platas, Craig A. Parish, Jenny M. Baxter, Javier Collado, Joann Huber, Karen Dorso, George K. Abruzzo, Antonio Gonzalez, Francisca Vicente, Maria Teresa Diez, Kenneth E. Wilson
Publikováno v:
Journal of Natural Products. 67:1900-1902
The isolation and structure elucidation of 1 from the Basidomycete fungus Baeospora myosura is described. This new ene-triyne antibiotic was most potent against Gram-positive bacteria, while it was less active against Gram-negative bacteria and a yea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d513aac2c6cf2eb51b750fb945cb4a1
https://doi.org/10.1021/np0497853
https://doi.org/10.1021/np0497853
Autor:
James L. Leighton, Jenny M. Baxter Vu
Publikováno v:
ChemInform. 42
Bishomoallylic benzoic hydrazides are prepared via reaction of silyl ketene imines with acylhydrazones in the presence of the chiral silane Lewis acid HSLA under conditions A) or B).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ce0de64d75e6c90d4877455c9e70516
https://doi.org/10.1002/chin.201150087
https://doi.org/10.1002/chin.201150087
Autor:
James L. Leighton, Jenny M. Baxter Vu
Publikováno v:
Organic letters. 13(15)
A new two-step synthesis of highly substituted pyrrolidines has been developed. Chiral silane Lewis acid promoted enantioselective Mannich reactions of silyl ketene imines with acylhydrazones may be used to access bishomoallylic benzoic hydrazides th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e15d5bf534b00334cc8688e2595c97d4
https://pubmed.ncbi.nlm.nih.gov/21749067
https://pubmed.ncbi.nlm.nih.gov/21749067
Publikováno v:
ChemInform. 42
The reactions allow efficient asymmetric access to α-aryl-β-hydrazido esters and α,α-disubstituted β-hydrazido nitriles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97e21cc07dd87736552883417e0b4c2c
https://doi.org/10.1002/chin.201122056
https://doi.org/10.1002/chin.201122056
Publikováno v:
Organic letters. 13(4)
Mannich reactions with chiral silicon Lewis acid activated acylhydrazones and α-aryl silyl ketene acetals and α-aryl,α-alkyl silyl ketene imines proceed efficiently and with good to excellent levels of both diastereoselectivity and enantioselectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce813c878903ea0ac8137884a6a0083a
https://pubmed.ncbi.nlm.nih.gov/21235253
https://pubmed.ncbi.nlm.nih.gov/21235253
Publikováno v:
ChemInform. 37
[reaction: see text] Herein we demonstrate functionalized enol tosylates to be robust substrates that undergo Suzuki-Miyaura, Sonogashira, and Stille cross-coupling reactions to provide stereodefined trisubstituted unsaturated esters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40c0f626b1167d20dccb3e999dc68fbf
https://doi.org/10.1002/chin.200614085
https://doi.org/10.1002/chin.200614085
Publikováno v:
ChemInform. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e6513005fcba2ff9f365e32f14f68f7
https://doi.org/10.1002/chin.200520078
https://doi.org/10.1002/chin.200520078