Bis-(dialkylamino)-cyclopropenylidene (BAC) Catalyzed Conjugate Addition of Nuleophiles to Para-Quinone Methides and Chalcones

dc.contributor.authorSingh, Gurdeep
dc.date.accessioned2017-07-18T07:31:20Z
dc.date.available2017-07-18T07:31:20Z
dc.date.issued2017-07-18
dc.description.abstractBis-(dialkylamino)-cyclopropenylidene (BAC) has been utilized as a BrØnsted base for the conjugate addition of C-nucleophiles to para-quinone methides and chalcones. This transformation occurs at mild conditions and is tolerant to a variety of functional groups. This protocol provides an easy and straightforward access to a set of diaryl and triarylmethanes in good to excellent yieldsen_US
dc.description.sponsorshipIISER-Men_US
dc.guideAnand, R.V.
dc.identifier.urihttp://hdl.handle.net/123456789/835
dc.language.isoenen_US
dc.publisherIISER-Men_US
dc.subjectChemistryen_US
dc.subjectNuleophilesen_US
dc.subjectp-quinone methidesen_US
dc.subjectBis-(dialkylamino)-cyclopropenylideneen_US
dc.subjectChalconesen_US
dc.titleBis-(dialkylamino)-cyclopropenylidene (BAC) Catalyzed Conjugate Addition of Nuleophiles to Para-Quinone Methides and Chalconesen_US
dc.typeThesisen_US

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
MP14012.pdf
Size:
5.77 MB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: