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Volumn 33, Issue 17, 1994, Pages 1729-1731

Synthesis of Cyclotheonamide B and Its Derivatives

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Indexed keywords

EID: 33750259615 PISSN: 05700833 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.199417291 Document Type: Article

Times cited : (45)

References (23)

2
- 0026795414
- For reassignment of stereochemistry and total synthesis of cyclotheonamide B, see
- (1992) J. Am. Chem. Soc. , vol.114 , pp. 6570
- Hagihara, M.¹ Schreiber, S.L.²

3
- 0027487010
- For the total synthesis of cyclotheonamide A, see
- (1993) J. Org. Chem. , vol.58 , pp. 5592
- Wipf, P.¹ Kim, H.²

6
- 0026716205
- (a) For the synthesis of fragments of cyclotheonamides
- (1992) Tetrahedron Lett. , vol.33 , pp. 3993
- Roth, P.¹ Metternich, R.²

7
- 0026752061
- (1992) Tetrahedron Lett. , vol.33 , pp. 4275
- Wipf, P.¹ Kim, H.²

8
- 84989522299
- (Proc. 2nd Jpn. Symp. Peptide Chem.), Ed.:, N. Yanaihara, Escom, Leiden
- (1993) Peptide Chemistry 1992 , pp. 72
- Deng, J.¹ Hamada, Y.² Shioiri, T.³

13
- 0028115578
- For aryl groups as the synthetic equivalent of carboxyl groups, see
- (1994) Tetrahedron , vol.50 , pp. 265
- Matsuura, F.¹ Hamada, Y.² Shioiri, T.³

15
- 0026553718
- 1H NMR spectra of the corresponding oxazolinones A: major isomer (syn): δ(5‐H) = 5.58 (J = 8.25 Hz); minor isomer (anti): δ(5‐H) = 5.09 (J = 6.59 Hz):,. (Formula Presented.)
- (1992) Tetrahedron Lett. , vol.33 , pp. 1411
- Poss, M.A.¹ Reid, J.A.²

17
- 33748638545
- (1990) J. Org. Chem. , vol.55 , pp. 1928
- Nuñez, M.T.¹ Martin, V.S.²

18
- 84989507168
- The corresponding vinylogous (R)‐tyrosine ester was obtained analogously in 89% yield (E:Z = 95:5). See also ref.[5c].

21
- 84989587065
- 3). The configurations of the hydroxyl functions in 15a and 15b were deduced from those of their precursors 5; see also ref.[10].

22
- 3042741556
- (1991) J. Am. Chem. Soc. , vol.113 , pp. 7277
- Dess, D.B.¹ Martin, J.C.²

23
- 84989587051
- −1under the same conditions. Since cyclotheonamide B was not available, the comparative study of the enzyme inhibition was not possible.

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