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C1COCC2C1O2

O[C@@H]1C[C@@H](C(c2ccccc2)c2ccccc2)OC[C@H]1NCc1ccc(F)cc1
Reaction #166114
(2S,4R,5R)-2-benzhydryl-5-(4-fluoro-benzylamino)-tetrahydropyran-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
O[C@H]1C[C@H](C(c2ccccc2)c2ccccc2)OC[C@@H]1NCc1ccc(F)cc1
Reaction #166115
(2R,4S,5S)-2-benzhydryl-5-(4-fluoro-benzylamino)-tetrahydropyran-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1C[C@@H](C(c2ccccc2)c2ccccc2)OC[C@H]1NCCc1ccc(F)cc1
Reaction #166116
(2S,4R,5R)-2-benzhydryl-5-[2-(4-fluorophenyl)-ethylamino]-tetrahydropyran-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
O[C@H]1C[C@H](C(c2ccccc2)c2ccccc2)OC[C@@H]1NCCc1ccc(F)cc1
Reaction #166117
(2R,4S,5S)-2-benzhydryl-5-[2-(4-fluorophenyl)-ethylamino]-tetrahydropyran-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1CO[C@H](C(c2ccccc2)c2ccccc2)C[C@H]1NCc1ccccc1
Reaction #166118
(3S,4R,6S)-6-benzhydryl-4-benzylamino-tetrahydropyran-3-ol
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CN[C@@H]2CO[C@H](C(c3ccccc3)c3ccccc3)C[C@H]2O)cc(OC)c1
Reaction #166119
(2S,4R,5R)-2-benzhydryl-5-(3,5-dimethoxy-benzylamino)-tetrahydropyran-4-ol
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN[C@@H]2CO[C@H](C(c3ccccc3)c3ccccc3)C[C@H]2O)c(OC)c1
Reaction #166120
(2S,4R,5R)-2-benzhydryl-5-(2,4-dimethoxybenzylamino)-tetrahydropyran-4-ol
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=N[C@@H]1CO[C@H](C(c2ccccc2)c2ccccc2)C[C@H]1O
Reaction #166121
(2S,4R,5R)-5-Azido-2-benzhydryl-tetrahydropyran-4-ol
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1CC[C@@H](C(c2ccccc2)c2ccccc2)OC1
Reaction #166128
33a
DOI: 10.6084/m9.figshare.5104873.v1
O[C@H]1CC[C@H](C(c2ccccc2)c2ccccc2)OC1
Reaction #166129
trans-(3S,6R)-6-benzhydryl-tetrahydro-pyran-3-ol
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1CC[C@H](C(c2ccccc2)c2ccccc2)OC1
Reaction #166130
(3R,6R)-6-benzhydryl-tetrahydropyran-3-ol
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
C[SiH](C)OC(C1OCC(N=[N+]=[N-])C(O)C1O)C(C)(C)C
Reaction #239229
DOI: 10.1039/C8SC04228D
COc1cccc(NC2COC(C(O[SiH](C)C)C(C)(C)C)C(O)C2O)c1
Reaction #297120
DOI: 10.1039/C8SC04228D
OC1CC(C(c2ccccc2)c2ccccc2)OCC1NCc1ccccc1
Reaction #300729
DOI: 10.1039/C8SC04228D
CC1OC(CC(=O)O)CC2=C1C(=O)c1c(O)cccc1C2=O
Reaction #310585
nanaomycin A
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=N[C@@H]1CCOC[C@H]1O
Reaction #332239
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1COC(C(c2ccccc2)c2ccccc2)CC1NCc1ccccc1
Reaction #374054
DOI: 10.1039/C8SC04228D
CCC1OC(OC)C2OC2C1=O
Reaction #374403
DOI: 10.1039/C8SC04228D
COc1cc(CNC2COC(C(c3ccccc3)c3ccccc3)CC2O)cc(OC)c1
Reaction #381578
DOI: 10.1039/C8SC04228D
OC1CC(C(c2ccccc2)c2ccccc2)OCC1NCCc1ccc(F)cc1
Reaction #397542
DOI: 10.1039/C8SC04228D
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