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semi-pinacol rearrangement (24) 24
chemistry, organic (13) 13
chemistry, multidisciplinary (11) 11
catalysis (7) 7
stereoselective construction (7) 7
semipinacol rearrangement (6) 6
total synthesis (6) 6
synthesis (5) 5
alpha-hydroxy epoxides (4) 4
asymmetric synthesis (4) 4
carbon (4) 4
ketones (4) 4
migration (4) 4
organic compounds (4) 4
semi‐pinacol rearrangement (4) 4
alcohols (3) 3
aldehydes (3) 3
alkenes (3) 3
allylic alcohols (3) 3
analysis (3) 3
cascade chemical reactions (3) 3
centers (3) 3
construction (3) 3
cyclization (3) 3
diels-alder reaction (3) 3
index medicus (3) 3
models, molecular (3) 3
natural-products (3) 3
organic-synthesis (3) 3
oxidation (3) 3
stereoisomerism (3) 3
-welwitindolinone-a isonitrile (2) 2
12,13-seco norditerpenoid alkaloid (2) 2
addition cascade (2) 2
alcohol (2) 2
alkaloids (2) 2
alkynes (2) 2
allylic compounds (2) 2
aromatization (2) 2
article (2) 2
asymmetric-synthesis (2) 2
c bond-cleavage (2) 2
catalysts (2) 2
catalyzed decarboxylative alkylation (2) 2
chemical properties (2) 2
chemical reactions (2) 2
chemical sciences (2) 2
chemistry, applied (2) 2
chemistry, physical (2) 2
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cyclohexenes - chemistry (2) 2
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efficient synthesis (2) 2
enantioselective construction (2) 2
ethers (2) 2
formal synthesis (2) 2
gold (2) 2
gold catalysis (2) 2
iodine (2) 2
isoflavonoid (2) 2
isomerization (2) 2
letter (2) 2
metal-free (2) 2
norditerpenoid alkaloid (2) 2
o-h insertion (2) 2
organic chemistry (2) 2
promoted rearrangement (2) 2
quaternary carbon (2) 2
reagents (2) 2
rearrangement (2) 2
rearrangements (2) 2
research (2) 2
rhodium (2) 2
rotenoid (2) 2
semipinacol rearrangements (2) 2
silyl enol ethers (2) 2
structure (2) 2
total-synthesis (2) 2
totalsynthese (2) 2
visible-light photocatalysis (2) 2
-cortistatin-a (1) 1
-deguelin (1) 1
1,5-hydrogen sigmatropic rearrangement (1) 1
12,13- seco norditerpenoid alkaloid (1) 1
2,3-aziridino alcohols (1) 1
[ chim.orga ] chemical sciences/organic chemistry (1) 1
[3+2] dipolar cycloaddition (1) 1
acetal (1) 1
acetals (1) 1
acid catalyst (1) 1
acyloin rearrangement (1) 1
adamantylideneadamantane (1) 1
alcohols - chemistry (1) 1
alcools (1) 1
aldehyde metathesis (1) 1
aldol (1) 1
aldol aldol process (1) 1
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alkaloids - chemical synthesis (1) 1
alkohole (1) 1
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Angewandte Chemie International Edition, ISSN 1433-7851, 05/2017, Volume 56, Issue 21, pp. 5858 - 5861
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 07/2018, Volume 54, Issue 58, pp. 8096 - 8099
Two photo-catalytic tandem alkyl radical addition/semipinacol rearrangement reactions of cycloalkanol-substituted styrenes with N-acyloxyphthalimides and... 
Journal Article
Chemical Communications, ISSN 1359-7345, 2018, Volume 54, Issue 58, pp. 8096 - 8099
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 01/2012, Volume 10, Issue 3, pp. 502 - 505
Under Lewis acid activation, the new alpha-hydroxy-spiro epoxide scaffold 1a underwent an original tandem Payne/Meinwald rearrangement affording the... 
ALDOL ALDOL PROCESS | TEDANOLIDES | SEMI-PINACOL REARRANGEMENT | ORGANIC-SYNTHESIS | STEREOSELECTIVE CONSTRUCTION | CHEMISTRY, ORGANIC | ETHER REARRANGEMENTS | CENTERS | PROMOTED REARRANGEMENT | C1-C-11 FRAGMENT | QUATERNARY CARBON | Organic chemistry | Chemical Sciences
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 04/2016, Volume 358, Issue 9, pp. 1392 - 1397
A highly regio‐ and stereoselective method to construct a broad range of 7‐oxabicyclo[2.2.1]heptanes, which proceeds through a sequential reaction involving... 
tandem reaction | farnesiferol C | asymmetric synthesis | gold catalysis | semi‐pinacol rearrangement | semi-pinacol rearrangement | GOLD | CHEMISTRY, ORGANIC | ALPHA | SESQUITERPENOIDS | REARRANGEMENT | INHIBITORS | CHEMISTRY, APPLIED | CATALYSTS | Synthesis | Catalysis | Organic compounds | Gold | Chemical synthesis | Heptanes | Isomerization | Alkynes | Synthesis (chemistry) | Construction | Asymmetry | Migration
Journal Article
Synthesis, ISSN 0039-7881, 03/2019, Volume 51, Issue 5, pp. 1139 - 1156
Abstract A general synthetic approach to rotenoids is described, featuring 1) stereospecific, group-selective 1,2-rearrangements of epoxy alcohols, and 2) S N... 
feature | rotenoid | CHEMISTRY, ORGANIC | IDENTIFICATION | CONSTITUTION | DEGUELIN | PINACOL-TYPE REARRANGEMENT | semi-pinacol rearrangement | INSECT TOXINS | isoflavonoid | (+/-)-DEGUELIN | ISOFLAVONOIDS | SNAr cyclization | TRIETHYLALUMINUM | total synthesis | ASYMMETRIC TOTAL-SYNTHESIS | CONCISE SYNTHESIS
Journal Article
ACS Catalysis, ISSN 2155-5435, 07/2017, Volume 7, Issue 7, pp. 4435 - 4440
Journal Article
Chemistry – An Asian Journal, ISSN 1861-4728, 09/2015, Volume 10, Issue 9, pp. 1874 - 1880
Journal Article
Synlett, ISSN 0936-5214, 11/2009, Volume 2009, Issue 18, pp. 3040 - 3042
Abstract The concise total synthesis of (±)-crinine was accomplished in 24% overall yield and eleven steps starting from an easily available allylic alcohol.... 
letter | Alkaloids | Semi?pinacol rearrangement | Aldol reaction | Aza-Michael reaction | Total synthesis | aldol reaction | ALKENES | AZA-COPE REARRANGEMENTS | aza-Michael reaction | EFFICIENT APPROACH | CRININE | ALLYLIC ALCOHOLS | alkaloids | CHEMISTRY, ORGANIC | semipinacol rearrangement | total synthesis
Journal Article
Asian Journal of Organic Chemistry, ISSN 2193-5807, 08/2019, Volume 8, Issue 8, pp. 1390 - 1393
Journal Article