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enantiocontrolled synthesis (140) 140
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-4-demethoxydaunomycinone (5) 5
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Tetrahedron, ISSN 0040-4020, 02/2017, Volume 73, Issue 6, pp. 809 - 818
Asymmetric synthesis of enantiopure cuparenoid sesquiterpenes ( )-α-cuparenone, ( )-cuparene and a formal synthesis of ( )-β-cuparenone was presented in this... 
Cuparenoids | Ring closing metathesis | Asymmetric synthesis | Meinwald rearrangement | OXIDATION | ENANTIOSELECTIVE SYNTHESIS | CHEMISTRY, ORGANIC | QUATERNARY CARBONS | ALDEHYDES | (+)-ALPHA-CUPARENONE | NATURAL ORDER CUPRESSALES | ENANTIOCONTROLLED SYNTHESIS | CONSTRUCTION | ALPHA-CUPARENONE | (-)-ALPHA-CUPARENONE
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 08/2017, Volume 82, Issue 15, pp. 8213 - 8219
A facile formal synthesis to aphanorphine and its analogue is described, featuring Rh-catalyzed cyclohydrocarbonylation of 2-aminodihydronaphthalene to the... 
ARYL RADICAL CYCLIZATION | ASYMMETRIC CONSTRUCTION | LACTAM PRECURSORS | FORMAL SYNTHESIS | NATURAL-PRODUCTS | ENANTIOCONTROLLED SYNTHESIS | CHEMISTRY, ORGANIC | BENZYLIC QUATERNARY CARBONS | TANDEM REACTION | ALKENE CARBOAMINATION | (-)-APHANORPHINE | Hydrocarbons | Usage | Chemical properties | Chemical synthesis | Methyl groups
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 01/2019, Volume 2019, Issue 4, pp. 788 - 802
This manuscript describes the enantioselective synthesis of the aminocyclitol moiety of the antibiotic hygromycin A in eight steps and 39 % overall yield from... 
Dihydroxylation | Biocatalysis | Asymmetric synthesis | Cyclitols | Amino alcohols | MICROBIAL OXIDATION | (-)-HYGROMYCIN | ASYMMETRIC-SYNTHESIS | CHEMISTRY, ORGANIC | ENANTIODIVERGENT SYNTHESIS | FURANOSIDE | ANTITREPONEMAL SUBSTANCE | ENANTIOCONTROLLED SYNTHESIS | BIOLOGICAL EVALUATION | AROMATICS
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 10/1999, Volume 121, Issue 41, pp. 9562 - 9573
Described is a study of the preparation, reactivity, and diastereoselectivity of chiral 1-amino-3-siloxy-1,3-butadienes in the Diels−Alder reaction. These... 
ROUTE | ACID | ENANTIOSELECTIVE SYNTHESIS | DIASTEREOFACIAL REACTIVITY | ALLYLIC ALCOHOLS | CYCLOADDITIONS | ENANTIOCONTROLLED SYNTHESIS | STEREOSPECIFIC SYNTHESIS | 2-AMINO-1,3-BUTADIENES | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | Synthesis | Siloxanes | Chirality | Research | Diels-Alder reaction | Enantiomers | Organic compounds
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
Synthesis, ISSN 0039-7881, 11/2015, Volume 47, Issue 22, pp. 3435 - 3450
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 09/2012, Volume 2012, Issue 26, pp. 4988 - 4995
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 05/2011, Volume 17, Issue 23, pp. 6304 - 6308
Strike while the iron is hot: A temperature‐guided diastereoselectivity switch has been observed in the desymmetrization of meso‐7‐azabicyclic alkadiene. Both... 
azabicycloheptane | aminocyclitols | desymmetrization | diastereoselectivity | synthetic methods | MICROBIAL OXIDATION | AMINOCYCLOHEXITOL | NUCLEOPHILIC-ADDITION | AZA SUGARS | CHEMISTRY, MULTIDISCIPLINARY | ENANTIOMERICALLY PURE | CYCLOADDITIONS | ENANTIOCONTROLLED SYNTHESIS | CATALYZED ASYMMETRIC DESYMMETRIZATION | DERIVATIVES | RATIONAL DESIGN | Strategy | Iron | Synthesis | Enantiomers | Strikes | Switches
Journal Article
Organic Letters, ISSN 1523-7060, 12/2000, Volume 2, Issue 25, pp. 4013 - 4015
Journal Article
Organic Letters, ISSN 1523-7060, 12/2011, Volume 13, Issue 24, pp. 6596 - 6599
Journal Article
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 12/2006, Volume 71, Issue 25, pp. 9519 - 9521
Journal Article
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