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Chemical Communications, ISSN 1359-7345, 04/2011, Volume 47, Issue 13, pp. 3828 - 3830
Journal Article
Chemical Communications, ISSN 1359-7345, 01/2011, Volume 47, Issue 13, pp. 3828 - 3830
The design of biologically inspired, multi-component cascade reactions enables the targeted synthesis of assorted structurally complex products. Similar to... 
Cascade control | Reaction control | Control | Synthesis | Catalysis | Cascades | Cascade chemical reactions
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 09/2005, Volume 70, Issue 19, pp. 7592 - 7604
Two formal total syntheses of the (−)-salicylihalamides, based on chiral pool approaches, are reported. d-Glucose and l-rhamnose were used to prepare advanced... 
CORE | HINDERED SECONDARY ALCOHOLS | MITSUNOBU REACTION | ORGANIC-SYNTHESIS | CYTOTOXIC MACROLIDES | PRODUCTS | SALICYLIHALAMIDE-A | CHEMISTRY, ORGANIC | (+)-APICULAREN-A | OLEFIN METATHESIS | Glucose | Stereoisomerism | Rhamnose | Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis | Amides | Chemical properties | Structure | Dextrose
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 09/2005, Volume 70, Issue 19, pp. 7592 - 7604
Journal Article
Organic Letters, ISSN 1523-7060, 10/2003, Volume 5, Issue 21, pp. 4007 - 4009
Journal Article
Organic Letters, ISSN 1523-7060, 10/2003, Volume 5, Issue 21, pp. 4007 - 4009
Two formal chiral pool syntheses of the (−)-salicylihalamides A and B were achieved from commercially available 1,2,5,6-diacetone-d-glucose and l-rhamnose. 
CORE | CHEMISTRY, ORGANIC | CYTOTOXIC MACROLIDES | SALICYLIHALAMIDE-A | Rhamnose - chemistry | Molecular Structure | Stereoisomerism | Glucose - analogs & derivatives | Glucose - chemistry | Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis
Journal Article
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