Elaboration of the Isochromane System of Stephaoxocanes Employing an Oxa-Pictet Spengler Type Cyclization
An approach to the synthesis of the isochromane moiety embodying the AC-ring system of the stephaoxocanes, by the use of an Oxa-Pictet Spengler type cyclization strategy, is reported.
Main Authors: | Carmem R. Bernardi, Teodoro S. Kaufman, Claudio C. Silveira, Marcos Cipulli |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2000-03-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/5/3/493/ |
Similar Items
-
Catalytic Enantioselective Approaches to the oxa-Pictet–Spengler Cyclization and Other 3,6-Dihydropyran-Forming Reactions
by: Zhengbo Zhu, et al.
Published: (2019-07-01) -
Synthetic Studies on Natural Stephaoxocanes. Elaboration of a Tetrahydrooxazaphenalene Potential Intermediate
by: Teodoro Saul Kaufman
Published: (2000-03-01) -
The Pictet-Spengler Reaction Updates Its Habits
by: Andrea Calcaterra, et al.
Published: (2020-01-01) -
Pictet-Spengler reaction-based biosynthetic machinery in fungi
by: Yan, W., et al.
Published: (2014) -
Pictet–Spengler-Based Multicomponent Domino Reactions to Construct Polyheterocycles
by: Jun-Duo Hu, et al.
Published: (2023-12-01)