Toward creation of a universal NMR database for stereochemical assignment: complete structure of the desertomycin/oasomycin class of natural products.
about
Total synthesis and evaluation of cytostatin, its C10-C11 diastereomers, and additional key analogues: impact on PP2A inhibitionIso-petromyroxols: novel dihydroxylated tetrahydrofuran enantiomers from sea lamprey (Petromyzon marinus).Marinisporolides, polyene-polyol macrolides from a marine actinomycete of the new genus MarinisporaRare Polyene-polyol Macrolides from Mangrove-derived Streptomyces sp. ZQ4BG.Caylobolide B, a macrolactone from symplostatin 1-producing marine cyanobacteria Phormidium spp. from Florida.Improved stereochemical analysis of conformationally flexible diamines by binding to a bisporphyrin molecular clip.INTEGRATED APPROACHES TO THE CONFIGURATIONAL ASSIGNMENT OF MARINE NATURAL PRODUCTSDereplication: racing to speed up the natural products discovery process.A minimalist NMR approach for the structural revision of mucoxin.Progressive-convergent elucidation of stereochemistry in complex polyols. The absolute configuration of (-)-sagittamide A.An Amidinohydrolase Provides the Missing Link in the Biosynthesis of Amino Marginolactone AntibioticsHeat Shock Protein-Inducing Property of Diarylheptanoid Containing Chalcone Moiety from Alpinia katsumadai.A New Fatty Acid from the Endolichenic Fungus Massarina sp
P2860
Q30484031-3EC06BA4-9CBD-48E3-84EB-8224770EF276Q30915679-83425B98-842E-48A9-A90A-7B6DAB5A8EECQ33398626-D7A4DA8F-4EC0-406C-83F5-DB22D17CE861Q33687163-B3E12945-8A25-4526-B677-1B0F31A08FB1Q34248745-37C0C8ED-C36E-4A0D-9865-2B4894563F8DQ34985541-A0AA1FA4-6A45-4581-91FC-DFBF5B88CA6DQ36960591-2F4028A6-48A6-411D-B772-41F6D0FE3D93Q38409890-06D16361-E7E9-40D2-889C-527D87B837EEQ40931483-CEB71566-26A5-4202-AAAC-B7CCDCA7833FQ41774318-2757EC7A-336C-4713-8DCC-1F0D4A130F22Q42544847-42352E31-E0FA-4244-829D-A83C618F08F1Q47640436-B7D4109C-19AA-4E97-AE8A-FC1A2EC0872CQ57965767-C3FAD6FD-C5D5-4A1C-825F-199006D7E581
P2860
Toward creation of a universal NMR database for stereochemical assignment: complete structure of the desertomycin/oasomycin class of natural products.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
Toward creation of a universal ...... cin class of natural products.
@en
Toward creation of a universal ...... cin class of natural products.
@nl
type
label
Toward creation of a universal ...... cin class of natural products.
@en
Toward creation of a universal ...... cin class of natural products.
@nl
prefLabel
Toward creation of a universal ...... cin class of natural products.
@en
Toward creation of a universal ...... cin class of natural products.
@nl
P2093
P356
P1476
Toward creation of a universal ...... cin class of natural products.
@en
P2093
P304
P356
10.1021/JA004154Q
P407
P577
2001-03-01T00:00:00Z