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halosulfonylation (12) 12
terminal alkynes (10) 10
chemistry, organic (7) 7
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Angewandte Chemie (International ed.), ISSN 1433-7851, 2017, Volume 56, Issue 33, pp. 9949 - 9952
β,β‐Disubstituted vinyl sulfones were obtained with complete regio‐ and stereocontrol in a multicomponent reaction involving alkynes, organoboronic acids, and... 
nickel | stereoselectivity | carbosulfonylation | sulfonyl radicals | vinyl radicals | VINYLSULFONES | ROOM-TEMPERATURE | VINYL SULFONES | TERMINAL ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | HALOSULFONYLATION | CHEMISTRY | ALKYNYLCARBONYL COMPOUNDS | STEREOSELECTIVE-SYNTHESIS | DERIVATIVES | CYCLIZATION | Nickel | Catalysts | Chlorides | Radicals | Sulfones | Alkynes
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 2017, Volume 359, Issue 5, pp. 841 - 847
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 2019, Volume 361, Issue 3, pp. 597 - 602
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 08/2017, Volume 82, Issue 16, pp. 8761 - 8768
A copper-catalyzed oxidative cyclization procedure has been developed for the production of 2-sulfonated 9H-pyrrolo­[1,2-a]­indol-9-ones via the direct... 
FUNCTIONALIZATION | VINYL SULFONES | ACIDS | PHENYL SULFONES | RADICAL CYCLIZATION | SULFONYL HYDRAZIDES | BIOLOGICAL EVALUATION | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | TERT-BUTYL HYDROPEROXIDE | HALOSULFONYLATION
Journal Article
Organic Letters, ISSN 1523-7060, 12/2018, Volume 20, Issue 23, pp. 7509 - 7513
Herein, a one-step chlorosulfonylation of alkynes via a photocatalytic redox process is described. A variety of commercially available sulfonyl chlorides can... 
ALKENES | VINYL SULFONES | CHLOROTRIFLUOROMETHYLATION | CHEMISTRY | CHLORIDES | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | HALOSULFONYLATION | MOLECULES
Journal Article
Journal of organic chemistry, ISSN 0022-3263, 01/2019, Volume 84, Issue 2, pp. 780 - 791
Novel acylamino-directed relay disubstitutions realize the sequential difunctionalizations of anilides (1) under mild and metal-free conditions for the first... 
FUNCTIONALIZATION | BOND NITRATION | ALKENES | INSERTION | REGIOSPECIFIC SYNTHESIS | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | OXIDATIVE DIFUNCTIONALIZATION | HALOSULFONYLATION | 1,2-DIFUNCTIONALIZATION | TRIFLUOROMETHYLATION
Journal Article
New journal of chemistry, ISSN 1369-9261, 2018, Volume 42, Issue 11, pp. 8752 - 8755
An efficient, molecular iodine-promoted MCR of alkynes and sulfonyl hydrazide for the synthesis of ( )-β-iodo vinylsulfone derivatives has been developed. A... 
ORGANIC-SYNTHESIS | ALKENES | CINNAMIC-ACIDS | VINYL SULFONES | EFFICIENT SYNTHESIS | SULFONYLHYDRAZIDES | TERMINAL ALKYNES | INHIBITORS | CHEMISTRY, MULTIDISCIPLINARY | HALOSULFONYLATION | WATER | Catalysts | Catalysis | Hydrazides | Chemical synthesis | Molecular chains | Iodine | Alkynes
Journal Article
Tetrahedron letters, ISSN 0040-4039, 2018, Volume 59, Issue 44, pp. 3950 - 3954
Journal Article
ACS Omega, ISSN 2470-1343, 12/2018, Volume 3, Issue 12, pp. 18002 - 18015
An operationally simple, efficient, and metal-/peroxide-free three-component reaction of alkynes, iodine, and sodium sulfinates has been developed for the... 
VINYLSULFONES | PROMOTED IODOSULFONYLATION | VINYL SULFONES | CROSS-ADDITION | AQUEOUS-MEDIUM | SULFONYLHYDRAZIDES | TERMINAL ALKYNES | DIMERIZATION | STEREOSELECTIVE-SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | HALOSULFONYLATION
Journal Article
by Bi, WZ and Ren, CY and Jia, LG and Xia, XY and Chen, X and Chen, XL and Zhao, YF
PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, ISSN 1042-6507, 2017, Volume 192, Issue 4, pp. 391 - 396
The present reaction provides a simple and convenient synthetic strategy to construct beta-iodovinyl sulfones through molecular iodine and DTBP (di-tert-butyl... 
VINYL SULFONES | alkynes | SULFONYLHYDRAZIDES | OXINDOLES | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | sodium benzenesulfinates | HALOSULFONYLATION | CHEMISTRY, INORGANIC & NUCLEAR | IODIDES | ALKENES | beta-Iodovinyl sulfones | CHLORIDES | molecular iodine | INHIBITORS
Journal Article
07/1995, ISBN 0471939706, 67
This chapter contains sections titled: Introduction One‐Component Methods Two‐Component Methods Three‐Component Methods Miscellaneous Methods References 
sulfur dioxide | sulfone rearrangements | sulfene reactions | halide substitution | halosulfonylation | Halide substitution | Halosulfonylation | Sulfone rearrangements | Sulfene reactions | Sulfur dioxide
Book Chapter
07/1995, ISBN 0471939706, 40
This chapter contains sections titled: Introduction One‐Component Methods Two‐Component Methods Three‐Component Methods Miscellaneous Methods References 
sulfone rearrangements | anilinosulfone rearrangement | isomerization | sulfene reactions | halosulfonylation | Halosulfonylation | Sulfone rearrangements | Anilinosulfone rearrangement | Isomerization | Sulfene reactions
Book Chapter
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