Diazo reagents with small steric footprints for simultaneous arming/SAR studies of alcohol-containing natural products via O-H insertion.
about
Radicals: Reactive Intermediates with Translational PotentialSimultaneous structure-activity studies and arming of natural products by C-H amination reveal cellular targets of eupalmerin acetate.Chemo- and site-selective derivatizations of natural products enabling biological studies.Total syntheses and biological reassessment of lactimidomycin, isomigrastatin and congener glutarimide antibiotics.Distinct metabolites for photoreactive L-phenylalanine derivatives in Klebsiella sp. CK6 isolated from rhizosphere of a wild dipterocarp sapling.An approach to the site-selective deoxygenation of hydroxy groups based on catalytic phosphoramidite transferSite-selective bromination of vancomycin.Color-Coded Super-Resolution Small-Molecule Imaging.Highly stereoselective C-C bond formation by rhodium-catalyzed tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor carbenoids and chiral allylic alcohols.Rapid cycloaddition of a diazo group with an unstrained dipolarophile.Chemoselective hydroxyl group transformation: an elusive target.Catalytic X-H insertion reactions based on carbenoids.Applications of Nonenzymatic Catalysts to the Alteration of Natural Products.Cyclopropanations of olefin-containing natural products for simultaneous arming and structure activity studies.Bioconjugation by native chemical tagging of C-H bonds.Identification of Small Molecule-binding Proteins in a Native Cellular Environment by Live-cell Photoaffinity Labeling.
P2860
Q28468198-6CD3893A-909A-46F5-A34E-A2C193EC84B0Q30579599-DAAD25CD-239D-425D-865C-58D54675BB9DQ33699233-BC187385-6993-48E0-B325-0C5619D969C3Q34339977-DAA6C351-F860-488F-AEC3-A5BDB37F7202Q34829994-137CFEB3-F6B5-4E55-AEC7-D94EA6D16C7BQ35871115-4DCC8D05-BD75-488E-9B77-417AF1BCC421Q35892305-445C4FB2-8BC9-4C3C-8146-B3406B2E186AQ35963668-7FDAB19F-1E10-4F81-A403-C1B0EBAD3C31Q36146600-C95A82B5-715C-498B-A8BD-5797998DE5C3Q37446492-8ED6FB00-ACD9-4F9A-8A1E-1461DAC1D9E8Q38018503-BA71A081-1B81-4E19-953C-239354361285Q38081361-075F7CE7-B6B0-45B9-8831-349955C25A79Q39350547-19624DE8-9F8B-48EA-9289-00815F0D7FD0Q41285029-6FC73EC8-02AD-460B-9A06-A5728932EC61Q41957203-1F3BAC2D-1967-400B-A563-E689CD1FC8B2Q51449764-77619CF5-5C2F-46AB-A768-2C28782CD3CB
P2860
Diazo reagents with small steric footprints for simultaneous arming/SAR studies of alcohol-containing natural products via O-H insertion.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
Diazo reagents with small ster ...... al products via O-H insertion.
@en
Diazo reagents with small ster ...... al products via O-H insertion.
@nl
type
label
Diazo reagents with small ster ...... al products via O-H insertion.
@en
Diazo reagents with small ster ...... al products via O-H insertion.
@nl
prefLabel
Diazo reagents with small ster ...... al products via O-H insertion.
@en
Diazo reagents with small ster ...... al products via O-H insertion.
@nl
P2093
P2860
P356
P1433
P1476
Diazo reagents with small ster ...... al products via O-H insertion.
@en
P2093
Daniel Romo
Qing-Li He
Shridhar Bhat
Supakarn Chamni
Yongjun Dang
P2860
P304
P356
10.1021/CB2002686
P577
2011-09-28T00:00:00Z