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Natural Product Research, ISSN 1478-6419, 10/2019, Volume 33, Issue 20, pp. 2995 - 3010
Journal Article
ORGANIC LETTERS, ISSN 1523-7060, 06/2013, Volume 15, Issue 12, pp. 3042 - 3045
An effective reflexive-Michael (r-M) reaction has been disclosed to access drug-like six-membered spirooxindoles in good yields and excellent... 
MULTIPLE STEREOCENTERS | ORGANOCATALYST | DIELS-ALDER REACTION | CONSTRUCTION | CHEMISTRY, ORGANIC | CARBONYL-COMPOUNDS | CONTIGUOUS STEREOCENTERS | SPIROCYCLIC OXINDOLES | CONCISE SYNTHESIS | DERIVATIVES | HIGHLY EFFICIENT
Journal Article
by Hu, ZL and Zhu, Y and Fu, ZQ and Huang, W
JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, 08/2019, Volume 84, Issue 16, pp. 10328 - 10337
Herein, an efficient route to synthesize 6-hydroxyl butyrolactams has been successfully developed via an N-heterocyclic carbene-catalyzed formal [3 + 2]... 
DIHYDROPYRIDINONE | CATALYSIS | ENANTIOSELECTIVE SYNTHESIS | FORMAL SYNTHESIS | AMINO | GAMMA-LACTAMS | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | CLAUSENAMIDE | CONCISE SYNTHESIS | ACCESS
Journal Article
Organic Letters, ISSN 1523-7060, 06/2009, Volume 11, Issue 12, pp. 2703 - 2706
Enantioenriched pyranones are important intermediates in the synthesis of natural products and the generation of compound libraries. A one-pot method for their... 
KETONES | CONCISE | 8A-EPI-SWAINSONINE | EPOXY ALCOHOLS | FURANS | DE-NOVO SYNTHESIS | KINETIC RESOLUTION | CHEMISTRY, ORGANIC | ALDEHYDES | STEREOSELECTIVE-SYNTHESIS | GLYCOSYLATION REACTION
Journal Article
Chinese Journal of Organic Chemistry, ISSN 0253-2786, 01/2018, Volume 38, Issue 1, pp. 221 - 227
As a characteristic structural motif of numerous biologically active natural products and new drugs, chiral indoline derivatives have attracted much attention... 
Indoline-2-carboxylate | Williams chiral auxiliary | Buchwald-Hartig coupling | Asymmetric synthesis | CONCISE | SPIROTRYPROSTATIN-A | ACID | STRATEGY | CHEMISTRY, ORGANIC | ENANTIOSPECIFIC TOTAL-SYNTHESIS | TEMPLATES | indoline-2-carboxylate | asymmetric synthesis | (+)-AJMALINE | VERSATILE | (+)-ASPIDOSPERMIDINE | ASPIDOSPERMA ALKALOIDS
Journal Article
Synlett, ISSN 0936-5214, 03/2009, Volume 2009, Issue 5, pp. 783 - 786
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 01/2010, Volume 75, Issue 2, pp. 498 - 501
Journal Article
ORGANIC CHEMISTRY FRONTIERS, ISSN 2052-4129, 08/2019, Volume 6, Issue 16, pp. 2916 - 2923
The asymmetric synthesis of polycyclic fluorinated proline derivatives has been accomplished by means of an intramolecular azomethine ylide cycloaddition with... 
CONCISE | DESIGN | ENANTIOSELECTIVE SYNTHESIS | PYRROLIDINES | 1,3-DIPOLAR CYCLOADDITION | CONSTRUCTION | BIOLOGICAL EVALUATION | CHEMISTRY, ORGANIC | GENERATION | 4-FLUOROPYRROLIDINE-2-CARBONITRILE | PROLINE
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 11/2015, Volume 56, Issue 46, pp. 6433 - 6435
Journal Article
by Li, CL and Yu, ZX
JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, 08/2019, Volume 84, Issue 16, pp. 9913 - 9928
Ring expansion of in situ generated cyclopropylmethyl cations via Wagner-Meerwein rearrangement to cyclobutanes is widely used in synthesis. However, the... 
CONCISE | 1,6-ENYNES | ENANTIOSPECIFIC RING EXPANSION | THERMOCHEMISTRY | ENANTIOCONTROLLED SYNTHESIS | CHEMISTRY, ORGANIC | CYCLOISOMERIZATION | CYCLOPROPYLIDENE ALCOHOLS | DERIVATIVES | EPOXIDATION
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 10/2016, Volume 81, Issue 20, pp. 9567 - 9575
The asymmetric (er > 99:1) total synthesis of (+)-anti- and (−)-syn-mefloquine hydrochloride from a common intermediate is described. The Sharpless asymmetric... 
CONCISE | KETONES | STEREOISOMERS | ABSOLUTE-CONFIGURATION | RESOLUTION | ALPHA-ALKYLATION | ASSIGNMENT | CHEMISTRY, ORGANIC | ALPHA,ALPHA-BISALKYLATION | EFFICIENT | EPOXIDATION | X-ray crystallography | Usage | Mefloquine | Hydroxylation | Chemical properties | Stereochemistry | Research | Chemical synthesis
Journal Article
JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, ISSN 0037-9980, 08/2017, Volume 75, Issue 8, pp. 821 - 830
Journal Article
Tetrahedron: Asymmetry, ISSN 0957-4166, 04/2014, Volume 25, Issue 6-7, pp. 497 - 502
The synthesis of the indolizidine alkaloid, (+)-lentiginosine, is described. A key feature of the preparative route is the efficient and stereoselective... 
POLYHYDROXYLATED ALKALOIDS | CONCISE TOTAL-SYNTHESIS | (-)-LENTIGINOSINE | CHEMISTRY, ORGANIC | CHEMISTRY, PHYSICAL | DIRECTED DIHYDROXYLATION | CHEMISTRY, INORGANIC & NUCLEAR | ABSOLUTE-CONFIGURATION | ALLYLIC ALCOHOLS | TRICHLOROACETAMIDES | STEREOSELECTIVE-SYNTHESIS | INHIBITORS | LENTIGINOSINE | Synthesis | Organic compounds
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2018, Volume 16, Issue 5, pp. 771 - 779
An efficient diastereoselective approach to access the 3-hydroxy-2,6-disubstituted piperidine scaffold 1 has been developed through the Mannich process... 
SECONDARY ALCOHOLS | CONCISE | PIPERIDINE ALKALOIDS | TETRAHYDROPYRIDINES | LEWIS-ACID | SEDUM ALKALOIDS | CHEMISTRY, ORGANIC | NUCLEOPHILIC-SUBSTITUTION REACTIONS | NONRACEMIC BUILDING-BLOCK | EFFICIENT | ACCESS | Ketones | Asymmetric synthesis | Direct reduction | Piperidine | Chemical synthesis | Modularity | Acetals
Journal Article
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