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

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1016/0040-4039(95)01153-9

Persistent URL (handle)

Persistent link

Cite this

@article{3559e41e3f9c4d4c81305579bde98247,

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",

year = "1995",

doi = "10.1016/0040-4039(95)01153-9",

language = "English",

volume = "36",

pages = "5963--5966",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "33",

}

TY - JOUR

T1 - Total synthesis of Cyclotheonamide B, a facile route towards analogues.

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.

UR - https://www.scopus.com/pages/publications/0029117006

UR - https://www.scopus.com/inward/citedby.url?scp=0029117006&partnerID=8YFLogxK

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

UN SDGs

Access to Document

Persistent URL (handle)

Other files and links

Fingerprint

Cite this