2 edition of stereoselective synthesis of clavularin A. found in the catalog.
stereoselective synthesis of clavularin A.
Yian Shi
Published
1987
.
Written in English
| The Physical Object | |
|---|---|
| Pagination | 60 leaves |
| Number of Pages | 60 |
| ID Numbers | |
| Open Library | OL18049118M |
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A stereoselective synthesis of clavularin a from 2-cycloheptenone. Tetrahedron Letters28 (22), DOI: /S(00)Author: James D. White, Yoshiyasu Fukuyama. SoS Stereoselective Synthesis Protecting Groups Spectroscopic Methods in Organic Chemistry A Predictable Enantioselective Total Synthesis of (+)-Clavularin A Full Text book review.
Heaney, Harry: Alkaloids: Chemical & Biological Perspectives, Volume 9. Huang, Xian; Wang, Jun-Hua: A Convenient and Stereoselective Synthesis of -Vinylseleno Zirconocenes and -Vinylic Selenol Esters Full Text PDF (31 kb).
An efficient formal total synthesis of (±)-clavukerin A was accomplished via a gold-catalyzed cycloisomerization of a 3-methoxy-1,6-enyne 5 as the key strategy followed by Rh-catalyzed.
The synthesis of tricholomenyn A is described via a route employing two palladium-catalysed Sonogashira coupling reactions; an efficient, stereoselective route to. Full text of "The Nitro Group in Organic Synthesis" See other formats.
An earlier review of antitumor and cytotoxic compounds from marine organisms which covered the literature into early was published in by Munro et al.
The current review is intended to provide a comprehensive review of the field from the beginning of to early Cited by: COVID campus closures: see options for getting or retaining Remote Access to subscribed contentCited by: the nitro group in organic synthesis ORGANIC NITRO CHEMISTRY SERIES Managing Editor Dr.
Henry Feuer Purdue University West Lafayette, Indiana USA EDITORIAL BOARD Hans H. Baer Ottawa, Canada. Biocatalysis in the pharmaceutical and biotechnological applications is an indispensable resource for organic chemists, biochemists, microbiologists, biochemical engineers, biotechnologists, medicinal chemists, pharmacologists, and upper-level undergraduate and graduate students in these disciplines.
There is today no such book that is focused on this particular, there is need for a book that covers catalytic asymmetric last book on the general topic of conjugate reactions in organic synthesis waspublished in and the discussion of stereoselective reactions is a small part.
