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A highly efficient route to taxotere by the β-Lactam Synthon Method
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title
A highly efficient route to taxotere by the β-Lactam Synthon Method
(English)
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main subject
docetaxel
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based on heuristic
inferred from title
author
Iwao Ojima
series ordinal
1
object named as
Iwao Ojima
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author name string
Chung Ming Sun
series ordinal
2
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Martine Zucco
series ordinal
3
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Young Hoon Park
series ordinal
4
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Olivier Duclos
series ordinal
5
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Scott Kuduk
series ordinal
6
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publication date
June 1993
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published in
Tetrahedron Letters
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volume
34
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issue
26
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page(s)
4149-4152
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cites work
Efficient and practical asymmetric synthesis of the taxol C-13 side chain, N-benzoyl-(2R,3S)-3-phenylisoserine, and its analogs via chiral 3-hydroxy-4-aryl-.beta.-lactams through chiral ester enolate-imine cyclocondensation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0040-4039%2800%2960514-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New and efficient approaches to the semisynthesis of taxol and its C-13 side chain analogs by means of β-lactam synthon method
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0040-4039%2800%2960514-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Synthesis of biologically active taxol analogues with modified phenylisoserine side chains
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0040-4039%2800%2960514-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0040-4039(00)60514-2
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Fatcat ID
release_o3tmhhyqw5cwpffjsbbp4aafra
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