Asset Details
Do you wish to reserve the book?
Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using IN/I-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using IN/I-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
Do you wish to request the book?
Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using IN/I-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Journal Article
Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using IN/I-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
2023
Overview
A green one-pot 2,3,6-trifunctionalization of N-alkyl/aryl indoles was achieved by adding three equivalents of N-Br sulfoximine to the indole solution. A variety of 2-sulfoximidoyl-3,6-dibromo indoles were prepared with 38–94% yields using N-Br sulfoximines as both brominating and sulfoximinating reagents. Based on the results of controlled experiments, we propose that a radical substitution involving 3,6-dibromination and 2-sulfoximination occurs in the reaction process. This is first time that 2,3,6-trifunctionalization of indole in one pot has been achieved.
Publisher
MDPI AG
Subject
