Enantiospecific Formation of trans-1,3-Disubstituted Tetrahydro-βcarbolines by the Pictet-Spengler Reaction and Conversion of cis Diastereomers into Their trans Counterparts by Scission of the C-1/N-2 Bond. -The factors which effect the stereoselective formation of trans-products in the Pictet-Spen
✦ LIBER ✦
Conformational Analysis of the cis - and trans -Adducts of the Pictet−Spengler Reaction. Evidence for the Structural Basis for the C(1)−N(2) Scission Process in the c is - to trans -Isomerization
✍ Scribed by Han, Dongmei; Försterling, F. Holger; Deschamps, Jeffrey R.; Parrish, Damon; Liu, Xiaoxiang; Yin, Wenyuan; Huang, Shengming; Cook, James M.
- Book ID
- 120884116
- Publisher
- American Chemical Society
- Year
- 2007
- Tongue
- English
- Weight
- 288 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0163-3864
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