The Michael reaction of a methyl 2-C-nitro-α-d-hex-2-enopyranoside: Preparation and structural determination of the adducts having the d-altro-, d-gluco, and d-manno configurations
- 16 April 1981
- journal article
- Published by Elsevier in Carbohydrate Research
- Vol. 91 (1) , 67-76
- https://doi.org/10.1016/s0008-6215(00)80992-1
Abstract
No abstract availableKeywords
This publication has 2 references indexed in Scilit:
- Stereochemistry of Nucleophilic Addition Reactions. 10. Preparation of 2-C-Diacetylmethyl and 2-C-Acetylmethyl Derivatives with the Altro, Gluco, and Manno Configuration from Methyl 4,6-O-Benzylidene-2,3-dideoxy-3-nitro-α-d-erythro-hex-2-enopyranosideBulletin of the Chemical Society of Japan, 1980
- Preparation of methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-dinitro-α-D-glucopyranoside and its selective conversion into the corresponding 2-nitro-2-enopyranosideCarbohydrate Research, 1980