Author: Jennifer A. ChampouxPublisher:
ISBN:
Category :
Languages : en
Pages : 74
Book Description
Progress Toward the Total Synthesis of Superstolide A
Author: Jennifer A. ChampouxStudies Towards the Total Synthesis of Superstolide A.
Author: Yuichi TatenoStudies Towards the Total Synthesis of Superstolide A and the Auriside Aglycon
Author: Angela Claire MackaySynthetic Studies Toward the Total Synthesis of Superstolides A and B
Author: Zhengmao HuaPublisher:
ISBN: 9781109864328
Category : Macrolide antibiotics
Languages : en
Pages : 536
Book Description
An alternative approach was developed for the synthesis of bicyclo [2.2.2) octane. The key reaction of this approach is an asymmetric Diels-Alder reaction employing 1,3-diene that derived from R-4-t-butyldimethyl-silyloxy-2-cyclohexen-one. We have successfully achieved full control of the facile and stereoselectivity of this novel Diels-Alder reaction. The product of this reaction, a bicyclo[2.2.2]octane, is a very useful building block, and this methodology is expected to be widely used in organic synthesis.
Progress Towards the Total Synthesis of Chlorothricolide
Author: Steven Edward HallPublisher:
ISBN:
Category : Diels-Alder reaction
Languages : en
Pages : 344
Book Description
The Total Synthesis of (+/- )-epoxysorbicillinol and Progress Toward the Total Synthesis of (+)-epoxysorbicillinol
Author: Brian Dean ThompsonProgress Towards the Total Synthesis of Ingenol and Jatrophatrione
Author: Scott Douglas EdmondsonPublisher:
ISBN:
Category :
Languages : en
Pages : 600
Book Description
Progress Toward the Total Synthesis of 14-isoazacamptothecin and Synthesis of Substituted Quinoline
Author: Ibrahim Danlami BoriPublisher:
ISBN:
Category :
Languages : en
Pages : 367
Book Description
Progress in Total Synthesis
Author: Sarah DanishefskyPublisher:
ISBN: 9781468481853
Category :
Languages : en
Pages : 280
Book Description
Progress in Total Synthesis
Author: Sarah DanishefskyPublisher: Springer
ISBN: 9780306500015
Category : Science
Languages : en
Pages : 0
Book Description
This series stemmed from a group of weekly seminars in our research group aimed at keeping its members abreast of recent developments in organic synthesis. The seminars tended to consist of several syntheses of natural products or related systems with particular emphasis on the general strategy inherent in the effort, new and interesting reactions which were utilized in the work, and specificity (or the lack of it) in arranging the relative stereochemistry of asymmetric centers and the geometry of double bonds. We found that natural products offered an attractive setting in which the larger science of organic chemistry could be put to crucial tests. A truly elegant synthesis is a major advance in that it epitomizes how an imaginative mastery of the course of organic reactions can achieve a sophisticated objective by an economy of operations. Indeed any successful synthesis of a reasonably complex product, however cumbersome and graceless, is an important event for those who delight in the problem-solving dimension of science.