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The Quest for Quinine: Those Who Won the Battles and Those Who Won the WarRabe Rest in Peace: Confirmation of the Rabe–Kindler Conversion ofd-Quinotoxine Into Quinine: Experimental Affirmation of the Woodward–Doering Formal Total Synthesis of QuinineNew Tricks in Amino Acid Synthesis: Applications to Complex Natural ProductsSynthesis and antibacterial properties of (-)-nor-platencin.Platensimycin and its relatives: a recent story in the struggle to develop new naturally derived antibiotics.Analytics of Quinine and its Derivatives.Metal-Catalyzed Asymmetric Michael Addition in Natural Product Synthesis.First chemo-enzymatic synthesis of the (R)-Taniguchi lactone and substrate profiles of CAMO and OTEMO, two new Baeyer-Villiger monooxygenases.Concise stereocontrolled formal synthesis of (+/-)-quinine and total synthesis of (+/-)-7- hydroxyquinine via merged Morita-Baylis-Hillman-Tsuji-Trost cyclization.Intermolecular radical addition to N-acylhydrazones as a stereocontrol strategy for alkaloid synthesis: formal synthesis of quinine.Synthesis of fluorogenic polymers for visualizing cellular internalization.Synthetic and Organocatalytic Studies of Quinidine Analogues with Ring-Size Modifications in the Quinuclidine Moiety.Organic synthesis in the Smith Group: a personal selection of a dozen lessons learned at the University of Pennsylvania.A Sequential Homologation of Alkynes and Aldehydes for Chain Elongation with Optional (13)C-Labeling.Metal-Free Synthesis of N-Aryl Amides using Organocatalytic Ring-Opening Aminolysis of Lactones.The Rabe amination after a century: direct addition of N-heterocycles to carbonyl compounds.Accelerating the semisynthesis of alkaloid-based drugs through metabolic engineering.Direct room-temperature lactonisation of alcohols and ethers onto amides: an "amide strategy" for synthesis.Die Jagd auf Chinin: Etappenerfolge und GesamtsiegeSynthesis and Antimicrobial Activity of 3-Cyano-4-imino-9-methoxy-4H-pyrimido [2,1-b] pyrimido [4,5-b] quinoline and 2-Substituted Derivatives
P2860
Q21032515-A380F4E4-D2DB-49D5-A257-19BFFBDCC0CAQ29031197-B77B8048-D785-4519-A1E4-07FC4677EE1CQ33918474-1E91BDF0-6CC9-48AB-8376-385CAC202179Q37461971-D53930E1-44D1-432B-9140-CB618A8F8C8BQ37909984-24DF8C64-B507-4387-850F-C8F50E7D6187Q38399873-E48D2373-D08B-4E0E-AD85-82D84C0D6E60Q39043176-DF5DD1C3-5B7D-4EBC-BBAA-1E23A35B99F6Q41186790-29768001-068E-4661-8F19-130C037D2F52Q41380483-54599F1C-EEC8-43E3-AE4B-1DB277C9BC85Q41908195-1DB7957E-6761-4C6C-A228-D228F22B2E1FQ42605906-E1F97059-4C1D-47BF-871F-BC81D4562485Q47281086-2A56D8AF-7139-43C4-B3A6-43B2A3D4A5EEQ47809845-6675F463-A905-4F1C-942B-4EAE9794D462Q48258270-BFEC24FF-E2A7-4009-90ED-DC6CAEE297ADQ48318078-714CB822-98BB-448F-ABC7-B8B26F6795A7Q49213036-AB4794C2-A7DD-4CD3-8974-DDB0FD19EF0EQ51003523-B695C284-7772-4405-80B1-532B6FFEDFD7Q51838871-A5D067AF-07C0-4B21-A534-D09DCF93FCB9Q55899564-B686DFD0-1F60-404E-A13B-66EA79827333Q59011043-2828A47B-AE07-4D61-87BA-11907CECF4D3
P2860
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
The first stereoselective total synthesis of quinine.
@en
The first stereoselective total synthesis of quinine.
@nl
type
label
The first stereoselective total synthesis of quinine.
@en
The first stereoselective total synthesis of quinine.
@nl
prefLabel
The first stereoselective total synthesis of quinine.
@en
The first stereoselective total synthesis of quinine.
@nl
P2093
P356
P1476
The first stereoselective total synthesis of quinine.
@en
P2093
Balkovec JM
Fujimoto RA
P304
P356
10.1021/JA004325R
P407
P577
2001-04-01T00:00:00Z