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A study towards the total synthesis of TAN1251B
Asnuzilawati Asari1, Hayes, Christopher J2.
A synthetic route towards the synthesis of TAN1251B was developed utilizing an alkylidene carbene insertion reaction as a key step to construct the quartenary centre. The α-hydroxylation of the 5,6-spirocyclic enone with iodosobenzene was successful to give a mixture of diastereomer compounds 20 and 21 in 1:1.2 ratios.
Affiliation:
- Universiti Malaysia Terengganu, Malaysia
- University of Nottingham, United Kingdom
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Indexed by |
MyJurnal (2021) |
H-Index
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6 |
Immediacy Index
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0.000 |
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0 |
Indexed by |
Web of Science (SCIE - Science Citation Index Expanded) |
Impact Factor
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JCR (1.009) |
Rank |
Q4 (Multidisciplinary Sciences) |
Additional Information |
JCI (0.15) |
Indexed by |
Scopus 2020 |
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CiteScore (1.4) |
Rank |
Q2 (Multidisciplinary) |
Additional Information |
SJR (0.251) |
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