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Synthesis of chlorogenin 6-O-a
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化学生物学导向的有机合成
期刊论文 164
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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
虎眼万年青皂甙OSW－1类型皂甙的
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
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