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Synthesis and investigation of intermediates in the E.C.E. mechanism

✍ Scribed by J.A. Harrison; D.W. Shoesmith


Book ID
104148473
Publisher
Elsevier Science
Year
1970
Weight
408 KB
Volume
28
Category
Article
ISSN
0022-0728

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πŸ“œ SIMILAR VOLUMES


Spectroelectrochemical studies of E.E. a
✍ Gary A. Gruver; Theodore Kuwana πŸ“‚ Article πŸ“… 1972 πŸ› Elsevier Science βš– 875 KB

This solvolytic mechanism is significant because it is one of the few where several workers ix 13 are now in agreement for the sequence and

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Stereoselective reduction of conjugated homopropargylic alcohols 1 followed by an elimination reaction, allows an efficient approach to stereodefined (E,E,E)-chlorotrienes. The interest of these chlorotrienes was illustrated by a stereocontrolled synthesis of navenone B and all E conjugated polyenes

ChemInform Abstract: Stereocontrolled Sy
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v