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ISSN 1359-7345, 4/2018, Volume 54, Issue 29, pp. 3598 - 36
A concise, asymmetric and divergent synthesis of lycoposerramine R and lycopladine A is presented. The synthesis features the palladium-catalyzed... 
Journal Article
Chemical Communications, ISSN 1359-7345, 2018, Volume 54, Issue 29, pp. 3598 - 3600
A concise, asymmetric and divergent synthesis of lycoposerramine R and lycopladine A is presented. The synthesis features the palladiumcatalyzed... 
(+)-LYCOPLADINE | LYCOPODIUM ALKALOIDS | FACILE | ASYMMETRIC TOTAL-SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | SKELETON | Chemical synthesis | Palladium
Journal Article
Angewandte Chemie, ISSN 1433-7851, 06/2013, Volume 52, Issue 23, p. 6015
Journal Article
Angewandte Chemie, ISSN 1433-7851, 06/2013, Volume 52, Issue 23, p. 6015
  A general approach toward the asymmetric total synthesis of various aspidosperma alkaloids includes the combination of a C-H bond activation with a Heck-type... 
Journal Article
Angewandte Chemie, ISSN 0044-8249, 04/2019, Volume 131, Issue 17, pp. 5810 - 5813
A concise and highly stereoselective total synthesis of the Daphniphyllum alkaloids (−)‐daphenylline has been accomplished. The synthesis was started from ( S... 
Totalsynthesen | Alkaloide | Daphenyllin | Diels-Alder-Cycloadditionen | Friedel-Crafts-Alkylierungen | Synthesis | Diels-Alder reaction | Organic compounds | Stereoselectivity | Alkaloids | Organic chemistry | Carvone | Chemical reactions | Chemical synthesis
Journal Article
ISSN 1477-0520, 6/2012, Volume 1, Issue 28, pp. 5452 - 5455
A stereocontrolled total synthesis of (−)-terpestacin has been achieved starting from ( R )-(−)-carvone as a chiral pool and ( E , E )-farnesol via a highly... 
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2019, Volume 58, Issue 17, pp. 5754 - 5757
A concise and highly stereoselective total synthesis of the Daphniphyllum alkaloids (−)‐daphenylline has been accomplished. The synthesis was started from ( S... 
Diels–Alder cycloaddition | Friedel–Crafts alkylation | daphenylline | total synthesis | alkaloids | DAPHNIPHYLLUM ALKALOIDS | Diels-Alder cycloaddition | Friedel-Crafts alkylation | CHEMISTRY, MULTIDISCIPLINARY | SKELETON | Alkaloids | Synthesis | Diels-Alder reaction | Organic compounds | Stereoselectivity | Organic chemistry | Carvone | Chemical reactions | Chemical synthesis
Journal Article
Nature Communications, ISSN 2041-1723, 05/2015, Volume 6, Issue 1, p. 7204
The structurally complex alkaloid gelsemine was previously thought to have no significant biological activities, but a recent study has shown that it has... 
GELSEMIUM-RANKINII | ACYLIMINIUM ION | MULTIDISCIPLINARY SCIENCES | STEREOCONTROLLED TOTAL-SYNTHESIS | RADICAL CYCLIZATIONS | INTERMEDIATE | OXINDOLE SYNTHESES | INTRAMOLECULAR REACTION | QUATERNARY CENTERS | (+/-)-GELSEMINE | DERIVATIVES | Stereoisomerism | Alkaloids - chemical synthesis | Cycloaddition Reaction
Journal Article
Organic Letters, ISSN 1523-7060, 02/2019, Volume 21, Issue 3, pp. 644 - 647
Starting from (R)-seudenol, an asymmetric synthesis of the DEFG rings of solanoeclepin A has been developed. The key transformations include the substrate... 
DICHLOROKETENE | SEGMENT | POTATO | MOIETY | ENANTIOSELECTIVE SYNTHESIS | CYCLOADDITIONS | CHEMISTRY, ORGANIC | A SYNTHESIS | STEREOCONTROLLED SYNTHESIS | INTRAMOLECULAR 2+2 PHOTOCYCLOADDITIONS | SUBSTRUCTURE
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 04/2018, Volume 54, Issue 29, pp. 3598 - 3600
A concise, asymmetric and divergent synthesis of lycoposerramine R and lycopladine A is presented. The synthesis features the palladium-catalyzed... 
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 08/2019, Volume 361, Issue 15, pp. 3514 - 3517
The total synthesis of (+)‐paniculatine, a unique structure in Lycopodium alkaloids, has been achieved starting from two known intermediates. The efficiency of... 
Hosomi | Michael addition | regiostereoselectivity | Sakurai | allylation | (+)-paniculatine | (-)-MAGELLANINE | (+)-MAGELLANINONE | Hosomi-Sakurai allylation | PANICULATINE-TYPE | TETRACYCLIC LYCOPODIUM ALKALOIDS | CHEMISTRY, ORGANIC | CHEMISTRY, APPLIED | CDE RING ANALOGS | Synthesis | Organic compounds | Alkaloids | Chemical reactions | Allyl compounds
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 02/2014, Volume 356, Issue 2‐3, pp. 340 - 346
Journal Article
Organic Letters, ISSN 1523-7060, 02/2011, Volume 13, Issue 3, p. 543
Journal Article
by Xu, B and Xun, W and Wang, TZ and Qiu, FYG
ORGANIC LETTERS, ISSN 1523-7060, 12/2018, Volume 20, Issue 23, pp. 7745 - 7745
Journal Article
Angewandte Chemie, ISSN 0044-8249, 06/2013, Volume 125, Issue 23, p. 6131
Journal Article
Angewandte Chemie, ISSN 0044-8249, 06/2013, Volume 125, Issue 23, p. 6131
Journal Article
Organic Letters, ISSN 1523-7060, 2017, Volume 19, Issue 18, pp. 4861 - 4863
Starting from (R)-citronellic acid and (R), seudenol, the total synthesis, of (+)-aplykurodinone-1, a highly degraded marine steroid, has been achieved in 11... 
DEGRADED STEROLS | FORMAL SYNTHESIS | APLYSIA-FASCIATA | ENE REACTION | CHEMISTRY, ORGANIC | APLYKURODINONE-1 | ENANTIOSELECTIVE TOTAL-SYNTHESIS
Journal Article
Organic Letters, ISSN 1523-7060, 02/2018, Volume 20, Issue 3, pp. 590 - 593
A chiral phosphoric acid catalyzed highly regio- and enantioselective Friedel-Crafts alkylation at the indole C7-position was developed via the introduction of... 
TUMOR PROMOTERS | C-H ARYLATION | ALPHA-KETIMINO ESTERS | DIHYDROTELEOCIDIN-B | NATURAL-PRODUCTS | RECEPTOR ANALYSIS | CARBOCYCLIC RING | BIOLOGICAL EVALUATION | CHEMISTRY, ORGANIC | AROMATIC-COMPOUNDS | LYNGBYATOXIN-A
Journal Article
Organic Letters, ISSN 1523-7060, 12/2011, Volume 13, Issue 24, pp. 6426 - 6428
Journal Article
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