nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A breakthrough in protein engineering of a glycosyltransferase
|
Reetz, Manfred T. |
|
|
|
1 |
p. 4-5 |
artikel |
2 |
A dancing nickel in asymmetric catalysis: Enantioselective synthesis of boronic esters by 1,1-addition to terminal alkenes
|
McCarty, Bethany J. |
|
|
|
1 |
p. 1-3 |
artikel |
3 |
Alternating current electrolysis: A photoredox catalysis mimic and beyond
|
Zhong, Junsong |
|
|
|
1 |
p. 4-10 |
artikel |
4 |
An asymmetric catalytic multi-component reaction enabled the green synthesis of isoserine derivatives and semi-synthesis of paclitaxel
|
Shi, Taoda |
|
|
|
1 |
p. 58-63 |
artikel |
5 |
An efficient method to synthesize N/O, O-difluoroboron complexes from alkynes
|
Chen, Yanmei |
|
|
|
1 |
p. 89-94 |
artikel |
6 |
An environmentally benign cascade reaction of 1,2,3-indantriones with ethyl 2-(pyridine-2-yl)acetates for site-selective synthesis of 5H-isochromeno[4,3-b]indolizin-5-ones
|
He, Haodan |
|
|
|
1 |
p. 54-61 |
artikel |
7 |
An environmentally benign multi-component reaction: Highly regioselective synthesis of functionalized 2-(diarylphosphoryl)-1,2-dihydro-pyridine derivatives
|
Li, Kun |
|
|
|
1 |
p. 59-68 |
artikel |
8 |
Asymmetric catalysis in synthetic strategies for chiral benzothiazepines
|
Wang, Haifeng |
|
|
|
1 |
p. 12-25 |
artikel |
9 |
Asymmetric catalytic hydrogenation of imines and enamines in natural product synthesis
|
Tang, Pei |
|
|
|
1 |
p. 26-41 |
artikel |
10 |
Azo group-enabled metal- and oxidant-free alkenyl C–H thiolation: Access to stereodefined tetrasubstituted acyclic olefins
|
Gao, Hao-Jie |
|
|
|
1 |
p. 67-70 |
artikel |
11 |
Biosynthesis of organic molecules via artificial cascade reactions based on cytochrome P450 monooxygenases
|
Li, Ren-Jie |
|
|
|
1 |
p. 52-59 |
artikel |
12 |
Brønsted acid-catalyzed 1,6-hydrophosphination of propargylic para-quinone methides and aza-para-quinone methides for the rapid construction of phosphorus-substituted quaternary carbon centers
|
Xiong, Ting |
|
|
|
1 |
p. 46-52 |
artikel |
13 |
Carbon dioxide cycle via electrocatalysis: Electrochemical carboxylation of CO2 and decarboxylative functionalization of carboxylic acids
|
Yang, Zixin |
|
|
|
1 |
p. 19-26 |
artikel |
14 |
Catalyst-free and atom-economical [4+3] cycloaddition of azadienes with cyclic azomethine imines for facile synthesis of 1,2,4-triazepines
|
Li, Lesong |
|
|
|
1 |
p. 57-61 |
artikel |
15 |
Catalyst-free and atom-economical 1,3-dipolar cycloaddition of C,N-cyclic azomethine imines: Facile synthesis of isoquinoline-fused spirocycles
|
Li, Lesong |
|
|
|
1 |
p. 69-78 |
artikel |
16 |
Catalytic asymmetric umpolung reaction of imines to synthesize isoindolinones and tetrahydroisoquinolines
|
Mou, Ze-Dong |
|
|
|
1 |
p. 70-73 |
artikel |
17 |
1,6-Conjugate addition of para-quinone methides using gem-diborylcarbanions: Practical access to gem-diborylalkanes bearing vicinal tertiary/quaternary stereocenters
|
Zi, Pu-Zhang |
|
|
|
1 |
p. 68-72 |
artikel |
18 |
Contemporary synthesis of bioactive cyclobutane natural products
|
Hui, Chunngai |
|
|
|
1 |
p. 1-6 |
artikel |
19 |
Controllable cross-coupling of thiophenols with dichloromethane mediated by consecutively paired electrolysis
|
Zeng, Ting |
|
|
|
1 |
p. 35-40 |
artikel |
20 |
Diastereoselective synthesis of spiro[chromane-3,3′-indolines] and spiro[chromane-3,2′-indenes] via DBU promoted formal [4 + 2]cycloaddition reaction
|
Wang, Daqian |
|
|
|
1 |
p. 53-58 |
artikel |
21 |
Efficient O-deallylation triggered by cobalt hydride-catalyzed oxidative hydrofunctionalization
|
Yin, Yun-Nian |
|
|
|
1 |
p. 64-66 |
artikel |
22 |
Electrochemical gold redox catalysis for selective oxidative arylation
|
Zhang, Shuyao |
|
|
|
1 |
p. 82-86 |
artikel |
23 |
Electrochemically mediated three-component synthesis of isothioureas using thiols as sulfur source
|
He, Muxue |
|
|
|
1 |
p. 41-45 |
artikel |
24 |
Electrode material promoted dehydrogenative homo-/cross-coupling of weakly activated naphthalenes
|
Liu, Siyuan |
|
|
|
1 |
p. 71-75 |
artikel |
25 |
Emerging radical rearrangement reactions: The 1,2-boron shift
|
McCallum, Terry |
|
|
|
1 |
p. 10-19 |
artikel |
26 |
Enantioselective [3 + 2] cycloadditions of terminal allenoates with β-sulfonyl-α,β-unsaturated ketones
|
Li, Xiuzheng |
|
|
|
1 |
p. 54-57 |
artikel |
27 |
Enhanced activity for aerobic oxidative of alcohols over manganese oxides stimulated with interstitial nitrogen doping
|
Ruan, Fei |
|
|
|
1 |
p. 38-44 |
artikel |
28 |
Examination of Milstein Ru-PNN and Rh-Tribi/Tetrabi dual metal catalyst for isomerization-linear-hydroformylation of C4 raffinate and internal olefins
|
Zhang, Runtong |
|
|
|
1 |
p. 40-45 |
artikel |
29 |
Highly efficient artificial light-harvesting systems constructed in aqueous solution for supramolecular photocatalysis
|
Sun, Guangping |
|
|
|
1 |
p. 32-37 |
artikel |
30 |
Iron-catalyzed indolo[2,3-c]quinoline synthesis from nitroarenes and benzylic alcohols/aldehydes promoted by elemental sulfur
|
Li, Rong |
|
|
|
1 |
p. 95-101 |
artikel |
31 |
Lewis acid-catalyzed [4 + 2] cycloaddition of 3-alkyl-2-vinylindoles with β,γ-unsaturated α-ketoesters
|
Sun, Yuwen |
|
|
|
1 |
p. 84-88 |
artikel |
32 |
Manganese/NaOPh co-catalyzed C2-selective C–H conjugate addition of indoles to α,β-unsaturated carbonyls
|
Wang, Zelong |
|
|
|
1 |
p. 66-69 |
artikel |
33 |
Metal-free synthesis of indolo[2,3-b]indoles through aerobic cascade dehydrogenative aromatization/oxidative annulation
|
Jiang, Pingyu |
|
|
|
1 |
p. 78-81 |
artikel |
34 |
Natural attapulgite supported nano-Ni catalysts for the efficient reductive amination of biomass-derived aldehydes and ketones
|
Zhang, Jia |
|
|
|
1 |
p. 42-50 |
artikel |
35 |
Near-perfect control of the regioselective glucosylation enabled by rational design of glycosyltransferases
|
Li, Jiao |
|
|
|
1 |
p. 45-53 |
artikel |
36 |
One-pot synthesis of salicylaldehyde containing biaryl frameworks via an aminocatalytic Diels-Alder-retro-Diels-Alder cascade reaction of ynals with 2-pyrones
|
Song, Xixi |
|
|
|
1 |
p. 66-69 |
artikel |
37 |
Organophotocatalyzed E and Z stereoselective C sp 3 - C sp 2 bond forming cross coupling reactions of carboxylic acids with β-aryl-vinyl halides
|
Huang, He |
|
|
|
1 |
p. 27-31 |
artikel |
38 |
Palladium-catalyzed cyclobutenation of aryl chlorides with norbornenes
|
Chen, Zhenkun |
|
|
|
1 |
p. 79-83 |
artikel |
39 |
Palladium-catalyzed sulfonylative coupling of benzyl(allyl) carbonates with arylsulfonyl hydrazides
|
Gong, Bozhen |
|
|
|
1 |
p. 110-115 |
artikel |
40 |
Perspectives on green synthesis and catalysis
|
Kim, Yiram |
|
|
|
1 |
p. 1-11 |
artikel |
41 |
Photocatalytic generation of 1,4-disubstituted 1,2,3-triazoles under metal, oxidant and azide-free conditions
|
Liu, Changhong |
|
|
|
1 |
p. 62-67 |
artikel |
42 |
Photomediated core modification of diaryl dihydrophenzines through three-component alkylarylation of alkenes toward organocatalyzed ATRP
|
Zhang, Yajun |
|
|
|
1 |
p. 35-41 |
artikel |
43 |
Primary amine-functionalized mesoporous phenolic resin as an effective and stable solid base catalyst for Knoevenagel reactions in water
|
Wang, Kaixuan |
|
|
|
1 |
p. 79-82 |
artikel |
44 |
Radical coupling of β-ketoesters and amides promoted by Brønsted/Lewis acids
|
Zhu, Joshua L. |
|
|
|
1 |
p. 70-74 |
artikel |
45 |
Recent advances in the syntheses of pyrroles
|
Shi, Tao |
|
|
|
1 |
p. 20-34 |
artikel |
46 |
Recent advances in the total synthesis of monoterpenoid indole alkaloids enabled by asymmetric catalysis
|
Liu, Xiao-Yu |
|
|
|
1 |
p. 25-39 |
artikel |
47 |
Recent advances in visible-light photoredox-catalyzed nitrogen radical cyclization
|
Wang, Pengzi |
|
|
|
1 |
p. 42-51 |
artikel |
48 |
Recent developments in highly efficient construction of P-stereogenic centers
|
Ye, Xinyi |
|
|
|
1 |
p. 6-18 |
artikel |
49 |
Robust NHC-palladacycles-catalyzed Suzuki−Miyaura cross-coupling of amides via C-N activation
|
Deng, Qinyue |
|
|
|
1 |
p. 75-78 |
artikel |
50 |
Self-assembled hexameric capsule: A highly β-selective O-glycosylation reaction enabled via proton wire mechanism
|
Kanagaraj, Kuppusamy |
|
|
|
1 |
p. 7-9 |
artikel |
51 |
Simple nucleophile/H2O promoted defluorinative ring-opening of gem-difluorocyclopropenes
|
He, Yimiao |
|
|
|
1 |
p. 14-19 |
artikel |
52 |
Skeletal contraction: A novel strategy to access multisubstituted cyclobutane
|
Xu, Chunfa |
|
|
|
1 |
p. 1-3 |
artikel |
53 |
Spirooxindoles: Recent report of green synthesis approach
|
Liandi, Agus Rimus |
|
|
|
1 |
p. 1-13 |
artikel |
54 |
Structure-guided protein design of fluoroacetate dehalogenase for kinetic resolution of rac-2-bromobutyric acid
|
Wang, Shu |
|
|
|
1 |
p. 60-65 |
artikel |
55 |
Sulfur-promoted, one-pot, and metal-free conversion of aromatic aldehydes to nitriles using an inorganic ammonium salt as the nitrogen source
|
Yin, Jiawen |
|
|
|
1 |
p. 46-53 |
artikel |
56 |
Sustainable electrochemical dearomatization for the synthesis of diverse 2, 3-functionalized indolines
|
Chen, Jun |
|
|
|
1 |
p. 25-30 |
artikel |
57 |
Synthesis of biheteroaryls via 2-methyl quinoline C(sp3)-H functionalization under metal-free conditions
|
Wang, Dahan |
|
|
|
1 |
p. 73-76 |
artikel |
58 |
Synthesis of tetrahydropyrrolothiazoles through one-pot and four-component N,S-acetalation and decarboxylative [3+2] cycloaddition
|
Ma, Xiaoming |
|
|
|
1 |
p. 74-77 |
artikel |
59 |
The roles of computer-aided drug synthesis in drug development
|
Jia, Pengfei |
|
|
|
1 |
p. 11-24 |
artikel |
60 |
Transition-metal-free trifluoromethylthiolation–acylation of arynes by insertion into the C–S bonds
|
Cao, Chengyao Kimmy |
|
|
|
1 |
p. 62-65 |
artikel |
61 |
Visible-light-enabled multicomponent synthesis of trifluoromethylated 3-indolequinoxalin-2(1H)-ones without external photocatalysis
|
Zhang, Letian |
|
|
|
1 |
p. 51-56 |
artikel |
62 |
Visible-light-induced decarboxylative alkynylation of carboxylic acids in batch and continuous flow
|
Qin, Longzhou |
|
|
|
1 |
p. 20-24 |
artikel |
63 |
Visible light-promoted enantioselective aerobic oxidation of pyrazolones by phase transfer catalysis
|
Wang, Yakun |
|
|
|
1 |
p. 102-109 |
artikel |
64 |
Visible-light-promoted tandem decarboxylation coupling/cyclization of N-aryl glycines with quinoxalinones: Easy access to tetrahydroimidazo[1,5-a]quinoxalin-4(5H)-ones
|
Tang, Zhen |
|
|
|
1 |
p. 31-34 |
artikel |