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. Author manuscript; available in PMC: 2012 Dec 16.
Published in final edited form as: J Org Chem. 2011 Jan 10;76(3):894–901. doi: 10.1021/jo102188q

Table 1.

NMR data (CDCl3) for faulkneryne A (4a)

no. δC, mult.a δH, mult. (J in Hz)b COSYb HMBC (H→C)
1 66.4, CH 3.72, dd (11.4, 6.2) H2 C2, C3
66.4, CH 3.78, dd (11.4, 3.8) H2 C3
2 64.0, CH 4.57, dd (6.2, 3.8) H1, H7 C1, C3, C4, C5
3 80.1, C
4 71.1, C
5 76.8, Cd
6 76.5, Cd
7 107.8, CH 5.49, d (10.9) H2, H8, H9 C3, C4, C5, C8, C9
8 149.5, CH 6.11, dt (10.9, 7.6) H7, H9 C6, C7, C9
9 30.9, CH2 2.33, (7.6) H7, H8, H10 C6, C7, C8, C11
10 28.7, CH2e 1.41, m H9, H11 C8, C9, C11
11 28.8, CH2e 1.30, m H10, H12 C12
12 28.9, CH2 1.31, m H11, H13 C11
13 28.6, CH2 1.39, m H12, H14 C14, C15
14 33.0, CH2 2.03, m (7.3) H13, H15, H16 C12, C15, C16
15 138.3, CH 6.17, dt (13.5, 7.3) H14, H16 C13, C14, C16
16 104.3, CH 6.01, d (13.5) H14, H15 C14, C15
a

125 MHz.

b

600 MHz.

c

Multiplicity assigned from HSQC.

d,e

Peaks may be interchanged.