A general procedure for the preparation of 11.–hydroxy gibberellins: synthesis of the methylesters of GA35 and 11.–hydroxy–GA7

Lewis N. Mander; Graham L. Patrick

doi:10.1016/S0040-4039(00)94572-6

A general procedure for the preparation of 11.–hydroxy gibberellins: synthesis of the methylesters of GA35 and 11.–hydroxy–GA7

Lewis N. Mander, Graham L. Patrick

Research output: Contribution to journal › Article › peer-review

18 Citations (Scopus)

Abstract

Hydroboration of gibberellin 9(11),16-dienes provides good access to 11β,17-diols from which 11β-hydroxy gibberellins may be prepared, eg. gibberellin A35 (2) and 11β-hydroxy gibberellin A7 (4), a new gibberellin from Lolium temulentum.

Hydroboration of gibberellin 9( 11),16-dienes provides good access to 11 β,17-diols from which 11 β-hydroxy gibberellins may be prepared, eg. gibberellin A35 (2) and 1lβ-hydroxy gibberellin A7 (4), a new gibberellin from Lolium temulentum.

Original language	English
Pages (from-to)	423-6
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	3
DOIs	https://doi.org/10.1016/S0040-4039(00)94572-6
Publication status	Published - 1990
Externally published	Yes

Access to Document

10.1016/S0040-4039(00)94572-6

Cite this

@article{3690b89dccab45bcaf01242f1c5770ea,

title = "A general procedure for the preparation of 11.–hydroxy gibberellins: synthesis of the methylesters of GA35 and 11.–hydroxy–GA7",

abstract = "Hydroboration of gibberellin 9(11),16-dienes provides good access to 11β,17-diols from which 11β-hydroxy gibberellins may be prepared, eg. gibberellin A35 (2) and 11β-hydroxy gibberellin A7 (4), a new gibberellin from Lolium temulentum.Hydroboration of gibberellin 9( 11),16-dienes provides good access to 11 β,17-diols from which 11 β-hydroxy gibberellins may be prepared, eg. gibberellin A35 (2) and 1lβ-hydroxy gibberellin A7 (4), a new gibberellin from Lolium temulentum.",

author = "Mander, {Lewis N.} and Patrick, {Graham L.}",

year = "1990",

doi = "10.1016/S0040-4039(00)94572-6",

language = "English",

volume = "31",

pages = "423--6",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "3",

}

TY - JOUR

T1 - A general procedure for the preparation of 11.–hydroxy gibberellins

T2 - synthesis of the methylesters of GA35 and 11.–hydroxy–GA7

AU - Mander, Lewis N.

AU - Patrick, Graham L.

PY - 1990

Y1 - 1990

N2 - Hydroboration of gibberellin 9(11),16-dienes provides good access to 11β,17-diols from which 11β-hydroxy gibberellins may be prepared, eg. gibberellin A35 (2) and 11β-hydroxy gibberellin A7 (4), a new gibberellin from Lolium temulentum.Hydroboration of gibberellin 9( 11),16-dienes provides good access to 11 β,17-diols from which 11 β-hydroxy gibberellins may be prepared, eg. gibberellin A35 (2) and 1lβ-hydroxy gibberellin A7 (4), a new gibberellin from Lolium temulentum.

AB - Hydroboration of gibberellin 9(11),16-dienes provides good access to 11β,17-diols from which 11β-hydroxy gibberellins may be prepared, eg. gibberellin A35 (2) and 11β-hydroxy gibberellin A7 (4), a new gibberellin from Lolium temulentum.Hydroboration of gibberellin 9( 11),16-dienes provides good access to 11 β,17-diols from which 11 β-hydroxy gibberellins may be prepared, eg. gibberellin A35 (2) and 1lβ-hydroxy gibberellin A7 (4), a new gibberellin from Lolium temulentum.

U2 - 10.1016/S0040-4039(00)94572-6

DO - 10.1016/S0040-4039(00)94572-6

M3 - Article

SN - 0040-4039

VL - 31

SP - 423

EP - 426

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 3

ER -

A general procedure for the preparation of 11.–hydroxy gibberellins: synthesis of the methylesters of GA35 and 11.–hydroxy–GA7

Abstract

Access to Document

Fingerprint

Cite this