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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b01142
Abstract: The development of a C(sp2)-C(sp3) cross-coupling reaction for rapid, parallel synthesis of analogues of two HIV NNRTI clinical candidates is described. This method allowed easy access to the C-ring space using a practical alkylation with…
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Keywords:
sp2 sp3;
development sp2;
hiv nnrti;
cross coupling ... See more keywords