NDLI: Stereoselective synthesis of sugar-fused (or 1,2-annulated) isochromans and isochromanones by using oxa-Pictet-Spengler reaction.

Content Provider	Semantic Scholar
Author	Verma, Ashish Kumar Chennaiah, Ande Dubbu, Sateesh Vankar, Yashwant D.
Copyright Year	2018
Abstract	A highly efficient stereoselective synthesis of sugar fused 1,2-annulated isochromans is reported by utilizing the oxa-Pictet-Spengler cyclization reaction. The process is found to be very general as both glucal and galactal derived C2-hydroxy-α-C-aryl glycosides lead to the target molecules in good yields. The utility of this strategy was extended to the synthesis of sugar fused isochromanones, which are bergenin type molecules.
Starting Page	8258
Ending Page	8262
Page Count	5
File Format	PDF HTM / HTML
DOI	10.1039/c8ob01698d
Alternate Webpage(s)	http://www.rsc.org/suppdata/c8/ob/c8ob01698d/c8ob01698d1.pdf
PubMed reference number	30204196
Alternate Webpage(s)	https://doi.org/10.1039/c8ob01698d
Journal	Medline
Volume Number	16
Issue Number	37
Journal	Organic & biomolecular chemistry
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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Stereoselective synthesis of sugar-fused (or 1,2-annulated) isochromans and isochromanones by using oxa-Pictet-Spengler reaction.