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hypervalent sulfonylimino-lambda-bromane (8) 8
chemistry, organic (5) 5
amination (4) 4
ethers (4) 4
c-h bonds (3) 3
catalysis (3) 3
chemistry, multidisciplinary (3) 3
functionalization (3) 3
organic-synthesis (3) 3
ambient-temperature (2) 2
amides (2) 2
amines (2) 2
c-h amination (2) 2
c-h functionalization (2) 2
chemical properties (2) 2
cyclic ethers (2) 2
index medicus (2) 2
regioselectivity (2) 2
ruthenium porphyrins (2) 2
stereoisomerism (2) 2
1,3-dicarbonyl compounds (1) 1
acetates - chemistry (1) 1
activation (1) 1
alkanes - chemistry (1) 1
alkylation (1) 1
alkylation of purines (1) 1
allylic amination (1) 1
amidation (1) 1
amide (1) 1
amin (1) 1
amination reactions (1) 1
amines - chemistry (1) 1
aminierung (1) 1
analysis (1) 1
antiviral activity (1) 1
arenes (1) 1
azo compounds - chemistry (1) 1
benzoxazoles (1) 1
benzylamines - chemistry (1) 1
benzylic positions (1) 1
bond formation (1) 1
bonds (1) 1
carbon - chemistry (1) 1
catalysts (1) 1
cf3 radical (1) 1
chemical bonds (1) 1
chemical compounds (1) 1
chemical-radical (1) 1
chemisches radikal (1) 1
chemistry, applied (1) 1
chloramine-t (1) 1
cleavage (1) 1
coupling (1) 1
cross coupling (1) 1
cytochrome-p-450 (1) 1
ch functionalization (1) 1
dehydrogenative coupling reaction (1) 1
dirhodium carboxylates (1) 1
efficient synthesis (1) 1
electroorganic chemistry (1) 1
ethyl acetate (1) 1
free radicals (1) 1
free route (1) 1
functional groups (1) 1
functionalisation (1) 1
funktionalisierung (1) 1
green chemistry (1) 1
hemiaminal ethers (1) 1
highly efficient (1) 1
history (1) 1
hiv (1) 1
hydrazine (1) 1
hydrocarbons (1) 1
hydrogen - chemistry (1) 1
hydrogen bonding (1) 1
hypervalent iodine (1) 1
imid (1) 1
imides (1) 1
insertion (1) 1
insertions (1) 1
intermolecular amination (1) 1
intramolecular amidation (1) 1
iod (1) 1
iodine (1) 1
lewis base activation (1) 1
light (1) 1
manganese porphyrins (1) 1
metal (1) 1
metal free (1) 1
metal-free conditions (1) 1
metals (1) 1
methods (1) 1
microwave-assisted conditions (1) 1
molecular structure (1) 1
molecular-oxygen (1) 1
n bond formation (1) 1
n, n -dibromosulfonamides (1) 1
n-dibromosulfonamides (1) 1
nitrene (1) 1
nitrene transfer (1) 1
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The Journal of Organic Chemistry, ISSN 0022-3263, 11/2012, Volume 77, Issue 22, pp. 9959 - 9969
Journal Article
CHEMISTRY LETTERS, ISSN 0366-7022, 12/2012, Volume 41, Issue 12, pp. 1672 - 1674
An intermolecular benzylic C-H bond amination utilizing the combination of chloramine-T and 12 without the aid of transition-metal catalysts has been... 
FUNCTIONALIZATION | FREE ROUTE | HYPERVALENT SULFONYLIMINO-LAMBDA-BROMANE | AMBIENT-TEMPERATURE | BENZOXAZOLES | CHEMISTRY, MULTIDISCIPLINARY | CYTOCHROME-P-450 | INSERTIONS
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 6/2018, Volume 16, Issue 24, pp. 4384 - 4398
Hemiaminal ether skeletons (HESs) are important backbones generally found in organic compounds. Compared to traditional functional group transformations,... 
ELECTROORGANIC CHEMISTRY | CHLORAMINE-T | ORGANIC-SYNTHESIS | C(SP)-H BONDS | METAL-FREE CONDITIONS | HYPERVALENT SULFONYLIMINO-LAMBDA-BROMANE | CHEMISTRY, ORGANIC | BOND FORMATION | NITRENE TRANSFER-REACTIONS | DEHYDROGENATIVE COUPLING REACTION | C-H AMINATION | Cross coupling | Metals | Insertion | Coupling | Ethers | Functional groups | Organic compounds
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 11/2014, Volume 356, Issue 16, pp. 3325 - 3330
We describe a new method for the intermolecular amination of the α‐CH bonds of ethers. A hypervalent iodine reagent was used as oxidant to enable the... 
hypervalent iodine | nucleosides | amination | radicals | CH functionalization | ARENES | HYPERVALENT SULFONYLIMINO-LAMBDA-BROMANE | CHEMISTRY, ORGANIC | AMBIENT-TEMPERATURE | IODINE | C-H functionalization | FUNCTIONALIZATION | BONDS | CHEMISTRY, APPLIED | TETRAHYDROFURAN | HISTORY | Transition metals | Synthesis | Amines | Amides | Catalysis | Ethers | Chemical compounds | Imides
Journal Article
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2016, Volume 14, Issue 3, pp. 844 - 848
The synthesis of 1,4-amino alcohols from THF treated with N-tosyliminobenzyliodinane (PhINTs) followed by a Grignard reagent under mild reaction conditions at... 
MICROWAVE-ASSISTED CONDITIONS | ROOM-TEMPERATURE | NITRENE TRANSFER | PORPHYRIN-CATALYZED AMIDATION | 1,3-DICARBONYL COMPOUNDS | HYPERVALENT SULFONYLIMINO-LAMBDA-BROMANE | CHEMISTRY, ORGANIC | CYCLIC ETHERS | C-H FUNCTIONALIZATION | DIRHODIUM(II) CARBOXYLATES | SINGLE-ELECTRON TRANSFER
Journal Article
Synlett, ISSN 0936-5214, 06/2016, Volume 27, Issue 9, pp. 1438 - 1442
A new metal-free amidation of ethers with N,N-dibromosulfonamides has been developed. A series of hemiaminal ethers or imines were prepared with moderate to... 
amidation | hemiaminal ethers | regioselectivity | ethers | nitrene | amides | N, N -dibromosulfonamides | ORGANIC-SYNTHESIS | RUTHENIUM PORPHYRINS | N-dibromosulfonamides | MANGANESE PORPHYRINS | HYPERVALENT SULFONYLIMINO-LAMBDA-BROMANE | CHEMISTRY, ORGANIC | ALLYLIC AMINATION | LEWIS BASE ACTIVATION | C-H BONDS | CYCLIC ETHERS | STEREOSELECTIVE-SYNTHESIS | AMINATION REACTIONS
Journal Article
中国化学快报:英文版, ISSN 1001-8417, 2018, Volume 29, Issue 1, pp. 61 - 64
A metal-free and light-promoted approach to the synthesis of N-9 alkylated purine nucleoside derivatives, via a CF3 radical triggered radical relay pathway,... 
Alkylation of purines | Regioselectivity | CF3 radical | Photochemistry | Metal free | radical | SIDE-CHAIN | HYPERVALENT SULFONYLIMINO-LAMBDA-BROMANE | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | HIGHLY EFFICIENT | PHOTOCATALYST | AMINATION | ETHERS | HIV | TEMPERATURE | ANTIVIRAL ACTIVITY | Purines | Usage | Light | Optical properties | Chemical properties | Free radicals (Chemistry) | Alkylation | Methods
Journal Article
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