Total synthesis of Cyclotheonamide B, a facile route towards analogues.

H.M.M. Bastiaans; J.L. van der Baan; H.C.J. Ottenheijm

doi:10.1016/0040-4039(95)01153-9

Total synthesis of Cyclotheonamide B, a facile route towards analogues.

H.M.M. Bastiaans, J.L. van der Baan, H.C.J. Ottenheijm

Research output: Contribution to Journal › Article › Academic › peer-review

Abstract

A flexible, convergent synthesis of Cyclotheonamide B (1b) was developed, starting from the constituent amino acids, using conventional benzyl-, t-butyl- and allyl-based protecting groups. By modification of the key intermediates, this approach allows the preparation of cyclotheonamide analogues. © 1995.

Original language	English
Pages (from-to)	5963-5966
Journal	Tetrahedron Letters
Volume	36
Issue number	33
DOIs	https://doi.org/10.1016/0040-4039(95)01153-9
Publication status	Published - 1995

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title = "Total synthesis of Cyclotheonamide B, a facile route towards analogues.",

abstract = "A flexible, convergent synthesis of Cyclotheonamide B (1b) was developed, starting from the constituent amino acids, using conventional benzyl-, t-butyl- and allyl-based protecting groups. By modification of the key intermediates, this approach allows the preparation of cyclotheonamide analogues. {\textcopyright} 1995.",

author = "H.M.M. Bastiaans and {van der Baan}, J.L. and H.C.J. Ottenheijm",

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AU - Bastiaans, H.M.M.

AU - van der Baan, J.L.

AU - Ottenheijm, H.C.J.

PY - 1995

Y1 - 1995

N2 - A flexible, convergent synthesis of Cyclotheonamide B (1b) was developed, starting from the constituent amino acids, using conventional benzyl-, t-butyl- and allyl-based protecting groups. By modification of the key intermediates, this approach allows the preparation of cyclotheonamide analogues. © 1995.

AB - A flexible, convergent synthesis of Cyclotheonamide B (1b) was developed, starting from the constituent amino acids, using conventional benzyl-, t-butyl- and allyl-based protecting groups. By modification of the key intermediates, this approach allows the preparation of cyclotheonamide analogues. © 1995.

U2 - 10.1016/0040-4039(95)01153-9

DO - 10.1016/0040-4039(95)01153-9

M3 - Article

SN - 0040-4039

VL - 36

SP - 5963

EP - 5966

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 33

ER -

Total synthesis of Cyclotheonamide B, a facile route towards analogues.

Abstract

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