Zobrazeno 1 - 10
of 14
pro vyhledávání: '"J. C. Head"'
Autor:
E. A. Saville‐Stones, J. C. Head, David S. Carver, N. S. Jennings, Stephen D. Lindell, Richard M. Turner
Publikováno v:
Tetrahedron. 50:6695-6704
Four carbocyclic analogues of the ribonucleoside coformycin, including the recently isolated natural product 2, have been synthesised in racemic form. The syntheses were achieved in a convergent and direct manner via palladium(0) catalysed coupling b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01a437d32cff6230429ce657269df26d
https://doi.org/10.1016/s0040-4020(01)89698-8
https://doi.org/10.1016/s0040-4020(01)89698-8
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e1b6c074d4f2014c462203a932ea76e
https://doi.org/10.1002/chin.199202312
https://doi.org/10.1002/chin.199202312
Autor:
E. A. Saville‐Stones, N. S. Jennings, David S. Carver, Richard M. Turner, Stephen D. Lindell, J. C. Head
Publikováno v:
ChemInform. 25
Four carbocyclic analogues of the ribonucleoside coformycin, including the recently isolated natural product 2, have been synthesised in racemic form. The syntheses were achieved in a convergent and direct manner via palladium(0) catalysed coupling b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c54199d7d345b0651e8b3709975040f6
https://doi.org/10.1002/chin.199441201
https://doi.org/10.1002/chin.199441201
Autor:
J C, Head
Publikováno v:
The Veterinary record. 146(26)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af812d47bf5980dd6fc8d800fa5bc207
https://pubmed.ncbi.nlm.nih.gov/10958492
https://pubmed.ncbi.nlm.nih.gov/10958492
Autor:
J C, Head
Publikováno v:
The Veterinary record. 135(24)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa761912af6806e9f862f6362dcc2d5d
https://pubmed.ncbi.nlm.nih.gov/7755792
https://pubmed.ncbi.nlm.nih.gov/7755792
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2603-2604
Cyclopentenyl allylic acetates have been prepared in diastereoisomerically enriched form by modification of the Prins reaction. Palladium(0) catalysed coupling between these allylic acetates and a heteroaromatic base provides a highly convergent and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4f758d5214cdac64bb259b261f67bd8
https://doi.org/10.1039/p19910002603
https://doi.org/10.1039/p19910002603
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :85-97
Three differently substituted unsaturated spiroacetals, two of which form part of the structure of avermectins A1b, B1b, A1a, and B1a, have been prepared by reaction of the appropriately substituted and chiral lithium acetylide with dibenzyl protecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9200b670f9e1cba985d227a3e1f8ad0
https://doi.org/10.1039/p19880000085
https://doi.org/10.1039/p19880000085
Publikováno v:
J. Chem. Soc., Chem. Commun.. :874-876
An enantiospecific synthesis of the dioxygenated spiroacetal moiety of milbemycins α7 and α8 has been developed from the appropriate epoxide and regioselective acylation of the C-23 alcohol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa186dfb74b24889a64b7aa6a1d9aa1e
https://doi.org/10.1039/c39860000874
https://doi.org/10.1039/c39860000874
Publikováno v:
ChemInform. 19
Three differently substituted unsaturated spiroacetals, two of which form part of the structure of avermectins A1b, B1b, A1a, and B1a, have been prepared by reaction of the appropriately substituted and chiral lithium acetylide with dibenzyl protecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc0f2c2ac4ea0485e072d51064209a2b
https://doi.org/10.1002/chin.198815372
https://doi.org/10.1002/chin.198815372
Publikováno v:
ChemInform. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27107da439df43cfdcedb3facffba0b7
https://doi.org/10.1002/chin.198729373
https://doi.org/10.1002/chin.198729373