Iodocyclisations reactions of Boc- and Cbz-protected N-allylguanidines
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In: Tetrahedron, Vol. 70, No. 29, 15.04.2014, p. 4412-4419.
Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Iodocyclisations reactions of Boc- and Cbz-protected N-allylguanidines
AU - Al-Shuhaib, Z.A.
AU - Al Shuhaiba, Z.
AU - Davies, D.H.
AU - Dennis, M.
AU - Evans, D.M.
AU - Fletcher, M.D.
AU - Franken, H.
AU - Hancock, P.
AU - Hollinshead, J.
AU - Jones, I.
AU - Kähm, K.
AU - Murphy, P.J.
AU - Nash, R.P.
AU - Rowles, R.
PY - 2014/4/15
Y1 - 2014/4/15
N2 - The cyclisation of mono-protected and bis-protected guanidines 8a–j under standard iodocyclisation conditions (I2/K2CO3) gave the guanidine heterocycles 9–25 via either a direct cyclisation or by a cyclisation/ring-contraction process, which could be controlled by careful selection of conditions.
AB - The cyclisation of mono-protected and bis-protected guanidines 8a–j under standard iodocyclisation conditions (I2/K2CO3) gave the guanidine heterocycles 9–25 via either a direct cyclisation or by a cyclisation/ring-contraction process, which could be controlled by careful selection of conditions.
UR - http://0-www.sciencedirect.com.unicat.bangor.ac.uk/science/article/pii/S0040402014004499
U2 - 10.1016/j.tet.2014.03.087
DO - 10.1016/j.tet.2014.03.087
M3 - Article
VL - 70
SP - 4412
EP - 4419
JO - Tetrahedron
JF - Tetrahedron
SN - 0040-4020
IS - 29
ER -