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虎眼万年青皂甙OSW－1类型皂甙的
  • 期刊名称：PCT/CN2005/000005
  • 时间：0
  • 相关项目：化学生物学导向的有机合成
作者： 俞飙，史炳锋,汤平平
同期刊论文项目
化学生物学导向的有机合成
期刊论文 164
同项目期刊论文
Chemoselective Deprotection of
Synthesis Studies Toward Chlor
Synthesis of 4-Azido-4-deoxy-
Total synthesis of tetrahydroq
Facile Synthesis of Ginsenosid
Preparation of N-aryl compound
Macrocyclization Studies and T
An aldol approach to the total
Facile entry to decahydroquino
Synthesis and cytotoxicities o
Facile conversion of spirostan
Total synthesis of lepadins B,
Synthesis of mono- and di-O-be
Two new flavonol glycosides fr
Design, Synthesis and In Vitro
Synthesis of 1,6,7-Trioxa-spir
Synthesis of the cytotoxic git
A facile preparation of uronat
A Sequential Reaction Process
Total Synthesis of Cyclomarin
Synthesis of Two Naturally Occ
Synthesis of tamarixetin and i
Synthesis of a typical glucuro
Total synthesis of CRM646-A an
Synthesis of the trisaccharide
Synthesis of AntimycinA3b
An efficient sequential reacti
L-Proline promoted Ullmann typ
A one-pot formal [4+2] cycload
Total synthesis and cytotoxici
Kinetic analysis of an efficie
RCM-Based Synthesis of (3R,4R,
Five new ocotillone-type sapon
Efficient Construction of Nove
Synthesis of 3-O-(β-d-xylopyr
Preparation of Enantiomericall
An efficient and tunable route
A selective inhibitor of elF2?
RCM Approaches toward the Dias
Seven new triterpenoids from S
Hydrogen-bonding-induced oligo
CuI/L-proline-catalyzed coupli
An unprecedented N-transacylat
Synthesis of Anemoclemoside B,
Synthesis of a S-linked hepara
Tetrahydroisoquinoline based s
First total synthesis of Camin
A formal [3+2] cycloaddition p
Total synthesis of cyclic tetr
Formation of aryl arylboronate
Polyphillin D is a potent apop
Chemical and biological charac
Toward synthesis of the regula
Application of a Regioselectiv
Effects of Polyphyllin D, a st
Characterization of the Chloro
Chiron Approach Towards a Conf
Synthesis of aryl azides and v
Synthesis of L-threofuranosyl
Mutiple-stage tandem mass spec
Four new dimeric triterpene gl
Synthesis of Benzene-Fuzed 1,7
A Facile Access to Chiral 4-Is
Hydrogen bonding and halogen b
An expeditious enantioselectiv
Synthesis of aryl sulfones via
Efficient entry to polysubstit
An Expeditious Route to the An
Total synthesis of halipeptin
Synthesis of chlorogenin 6-O-a
On the susceptibility of organ
Total Synthesis of Cyclodepsip
Structure–activity relationsh
Bromoetherification-based stra
Synthesis of a 5-oxo-2-tetrahy
Co-recycling of MT1-MMP and MT
Design of wide-spectrum inhibi
Synthesis of 5,6-dihydro-OSW-1
Halogen Bonding and Hydrogen B
Mild Ullmann-type biaryl ether
Amino acid promoted CuI-cataly
Parallel Fragment Assembly Str
Synthesis of a Tetra-deuterium
One pot glycosylation for the
An Efficient Enantioselective Synthesis of Blastmycinone
Resveratrol glucuronides as th
Andrographolide attenuates inf
OSW saponins: facile synthesis
Structural determination of a
CuI/N,N-dimethylglycine-cataly
An Expeditious Synthesis of No
Synthesis of bidesmosidic dihy
Selective inhibition of matrix
Total syntheses of halipeptins
Mild and Non-Racemization Cond
An Iterative Acetylene-Epoxide
Total Synthesis of Clavepictin
Aryl C-glycosylation of phenol
An in vitro selection system f
Diastereoselective aldol react
基于非生物折叠体的分子识别
Synthesis of a 1,2,7,8-tetraoxa-spiro[5.5]undecane
Synthesis of 15-demethyl brefeldin A and its 7-epi isomer
外消旋木榄醇甲的简捷合成
关于茎点霉联烯酸丙的绝对构型
两个单环有机过氧化物的合成
抗霉素合成概览
犬尿氨酸羟化酶选择性抑制剂L-3-(邻甲氧基苯甲酰基)丙氨酸的简捷合成
An Efficient Synthesis of Selective Human NR2A Antagonist NVP-AAM077
Solvent-switchable Acetalization by Yb（OTf）3-Catalyzed Procedures
Conversion of N-Acyl-4-phenyl/benzyl-oxazolidine-2-thiones into Thiol Esters in the Presence of EtSH-K2CO3
Synthesis of 1,2-Dioxane Type Antimalarial Peroxides
Synthesis and in vino Antimalarial Activity of Several Simple Analogues of Peroxyplakoric Acid
Synthesis of Potential Inhibitiors for Stat-3 Dimerization
Synthesis of a Nitro Analogue of Plakoric Acid
羰基保护基团的新进展
Brefeldin A全合成研究新进展
N-Unsubstituted and N-Arylated Fulleropyrrolidines： New Useful Building Blocks for C60 Functionalization
Self-assembly of Hydrazide-based Heterodimers Driven by Hydrogen Bonding and Donor-Acceptor Interaction
Hydrogen Bonded Semi-Rigidified Bispyridyl-Incorporating Aryl Amide Oligomers： Efficient ＂C＂-Styled Receptors for Aliphatic Ammoniums, a Remarkable Protonation Effect and Chiral Induction