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Vol. 2, No. 2 Smart Blocs™
Download PDF version (1.03 MB)
Introduction / Aldehydes / Brominated Compounds / Related Products / Reference Books
Aldehydes
Heterocycles / Boronic Acids / Salicylaldehyde-like / Acids & Esters / Arylaldehydes Supported Reagents / CHO Functionalized Resins / Aldehyde Scavengers
Heterocycles
32,844-8
C4H4N2O
1g
|
45,612-8
C4H4N2O
1g; 5g
|
15,262-5
C5H3BrOS
5g; 25g; 100g
|
28,345-2
C5H3BrOS
5g; 25g
|
43,398-5
C5H3BrO2
1g; 10g
|
P7,340-4
C5H5NO
5g; 25g; 100g
|
39,215-4
C5H6N2O
5g
|
52,569-3
C6H4BrNO
1g; 10g
|
H4,080-7
C6H6O3
250mg; 1g; 5g
|
NEW 53,306-8
C7H7NO2
5g
|
NEW 55,988-1
C8H11ClN2O
25g
|
NEW 51,874-3
C9H6BrNO
5g
|
NEW 53,307-6
C9H6ClNO
5g
|
49,344-9
C9H6O2
1g; 5g
|
12,944-5
C9H7NO
5g; 25g
|
51,383-0
C9H7NO
5g
|
39,011-9
C10H6ClNO
1g; 10g
|
40,202-8
C10H7NO3
1g
|
44,440-5
C10H8N2O
5g
|
NEW 13,413-9
C10H9NO
1g; 5g
|
26,243-9
C10H9NO
25g; 100g
|
51,112-9
C10H9NO
5g
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M1,494-3
C10H9NO2
100mg; 1g
|
NEW 56,593-8
C11H8OS
1g; 5g
|
37,577-2
C11H9NO2
1g; 5g
|
TOP
Boronic Acids
TOP Salicylaldehyde-like
26,181-5
C7H4Cl2O2
5g; 25g
|
13,728-6
C7H5BrO2
25g; 100g
|
NEW 51,677-5
C7H5BrO2
5g
|
34,606-3
C7H5ClO2
500mg
|
44,770-6
C7H5ClO2
5g; 25g
|
31,980-5
C7H5FO2
250mg; 1g
|
NEW 52,627-4
C7H5FO2
1g
|
14,432-0
C7H5NO4
5g; 25g
|
15,616-7
C7H5NO4
1g; 10g
|
27,535-2
C7H5NO4
5g; 25g
|
NEW 52,742-4
C7H5NO4
1g; 5g
|
H4,810-7
C7H5NO4
5g; 25g
|
14,408-8
C7H6O2
50g; 250g
|
H1,980-8
C7H6O2
15g; 100g; 500g
|
S35-6
C7H6O2
100g; 500g; 1kg
|
NEW 52,681-9
C8H7FO3
1g
|
43,408-6
C8H7NO5
1g; 5g
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N2,800-0
C8H7NO5
5g; 25g
|
31,691-1
C8H8O2
1g
|
44,455-3
C8H8O2
1g; 5g
|
45,466-4
C8H8O2
1g; 5g
|
12,080-4
C8H8O3
10g; 100g; 500g
|
14,368-5
C8H8O3
25g; 100g
|
14,686-2
C8H8O3
1g; 5g; 10g
|
16,069-5
C8H8O3
1g; 5g; 25g
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V110-4
C8H8O3
2g; 100g; 500g
|
14,039-2
C9H10O2
1g; 5g
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12,809-0
C9H10O3
5g; 100g
|
16,098-9
C9H10O3
50g
|
13,879-7
C9H10O4
250mg; 1g
|
25,871-7
C9H10O4
250mg; 1g
|
39,293-6
C9H10O4
250mg; 1g
|
S760-2
C9H10O4
5g; 25g; 100g
|
55083
C10H7NO2
1g; 5g
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H4,535-3
C11H8O2
25g; 100g; 500g
|
22,568-1
C11H15NO2
5g; 25g
|
TOP Acids & Esters
G1,060-1
C2H2O3
10g; 25g; 100g
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47723
C3H5NO3
5g
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28,718-0
C4H6O3
1ml; 5ml
|
42,158-8
C5H5NO4
5g; 25g
|
15,727-9
C7H10O3
5g; 10g
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68259
C7H10O3
50ml; 250ml
|
12,491-5
C8H6O3
10g; 25g; 100g
|
23,279-3
C8H6O3
1g; 5g
|
11,601-7
C8H6O3
25g; 100g
|
24,474-0
C9H8O3
1g, 5g
|
47749
C9H8O3
1g; 5g
|
15,215-3
C9H8O4
25g; 100g
|
47743
C9H8O4
5g; 25g
|
17,876-4
C10H8O3
1g; 5g; 25g
|
48,376-1
C10H17NO3
1g
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48,378-8
C10H17NO3
1g
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TOP Arylaldehydes
TOP
Supported Reagents
| 35,982-3 |
Chromic acid, polymer-supported, 20-50 mesh, ca. 2.5 mmol/g |
5g; 25g; 100g |
|
Polymer-supported reagent for the clean oxidation of primary and secondary alcohols to carbonyl compounds in high yields.1,2 Reagent for the synthesis of aldehydes and ketones from allylic and benzylic halides.3
References:
- Cainelli, G. et al. J. Am. Chem. Soc. 1976, 98, 6737.
- Wade, L.G.; Stell, L.M. J. Chem. Educ. 1980, 57, 438.
- Cardillo, G. et al. Tetrahedron Lett. 1976, 3985.
|
| 32,864-2 |
Borohydride, polymer-supported (Amberlite IRA-400), 20-50 mesh, ca. 2.5 mmol/g |
25g; 100g; 250g |
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Reduce aldehydes and ketones to alcohols.1
References:
- Yoon, N.M. et al. Tetrahedron Lett. 1983, 24, 5367.
|
TOP
CHO Functionalized Resins
| The following resins are useful for the solid-phase preparation of secondary sulfonamides, amides, ureas, carbamates, and feature dilute acid labile linkers.1-7 |
| 51,644-9 |
AMEBA resin, 1% DVB, 100-200 mesh, 1.0-1.5 mmol/g |
1g; 5g; 25g |
| 53,821-3 |
4-Benzyloxy-2,6-dimethoxybenzaldehyde, polymer-bound, 1% DVB, 100-200 mesh, 1.0-1.5 mmol/g |
1g; 5g; 25g |
| 51,627-9 |
3-Formyl-1-indoleacetic acid, polymer-bound, 1% DVB, 200-400 mesh, ca. 1.0 mmol/g |
1g; 5g; 25g |
| 53,242-8 |
Formylpolystyrene, 2% DVB, 100-200 mesh, 2.0-3.0 mmol/g |
1g; 5g; 25g |
References:
- Wilson, T.W. et al. Tetrahedron Lett. 1997, 38, 7151.
- Sarantakis, D. et al. Tetrahedron Lett. 1997, 38, 7325.
- Flygare, J.A. et al. J. Org. Chem. 1998, 63, 196.
- Bilodeau, M.T. et al. J. Org. Chem. 1998, 63, 2800.
- Estep, K.G. et al. J. Org. Chem. 1998, 63, 5300.
- Yan, B. et al. J. Comb. Chem. 2000, 2, 66.
- Cossey, J. et al. J Org. Chem 2001, 66, 7195.
TOP
Aldehyde Scavengers
| Selectively remove excess reagent and/or impurities using these scavenger resins.1-3 |
| 47,209-3 |
Ethylenediamine, polymer-bound, 1% DVB, 200-400 mesh, 2.5-3.0 mmol/g |
5g; 25g |
| 53,791-8 |
3-(Ethylenediamino)propyl-functionalized silica gel, 200-400 mesh, ca. 2.5 mmol/g |
5g; 25g; 100g |
| 47,367-7 |
Poly(styrene-co-divinylbenzene), aminomethylated, 2% DVB, 200-400 mesh, ca. 4 mmol/g |
5g; 25g |
| 36,425-8 |
3-Aminopropyl-functionalized silica gel, 200-400 mesh, ca. 1.0 mmol/g |
10g; 50g; 250g |
| 51,620-1 |
Sulfonyl amide, polymer-supported, 1% DVB, 100-200 mesh, 1.5-2.0 mmol/g |
5g; 25g |
| 53,793-4 |
2-Ethyl-benzenesulfonamide-functionalized silica gel, 200-400 mesh, 0.6-0.9 mmol/g |
5g; 25g; 100g |
| 53,232-0 |
p-Toluenesulfonyl hydrazide, polymer-bound, 1% DVB,100-200 mesh, ca. 2.5 mmol/g |
1g; 5g; 25g |
| 55,259-3 |
2-(4-Toluenesulfonyl hydrazino)ethyl functionalized silica gel, 200-400 mesh, ca. 2.0 mmol/g |
5g; 25g; 100g |
References:
- Flynn, D.L. et al. J. Am. Chem. Soc., 1997, 119, 4874.
- Chen, J., et al. Tetrahedron Lett. 1999, 40, 9195.
- Kaldor, S.W. et al. Tetrahedron Lett. 1996, 37, 7193.
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