Search More · GCI-TPs

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Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

12 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

C(=O)(C(O)=O)O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

C(CCC(=O)C(=O)O)(=O)C(O)=O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

C(CC(C(O)O)O)O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

But-1-ene-1,1,4-triol

C(CC=C(O)O)O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

7 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

Previewing top 10 entries. If you want the full results, please use the download button above.

Upstream Precursor

ZVAFCKLQJCZGAP-UHFFFAOYSA-N

Boc-(2S,3S)-3-amino-2-hydroxy-3-phenylpropionic acid

CC(C)(C)OC(=O)NC(C(C(=O)O)O)C1=CC=CC=C1

Environmental

Product

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Upstream Precursor

IBDIOGYTZBKRGI-UHFFFAOYSA-N

tert-Butyl (2-hydroxy-1-phenylethyl)carbamate

C(C(C1=CC=CC=C1)NC(=O)OC(C)(C)C)O

Environmental

Product

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Upstream Precursor

PEVGKAAGTGDOGA-UHFFFAOYSA-N

Tert-butyl N-(2-oxo-1-phenylethyl)carbamate

CC(C)(C)OC(=O)NC(C=O)C1=CC=CC=C1

Abiotic

Product

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Upstream Precursor

PEVGKAAGTGDOGA-UHFFFAOYSA-N

Tert-butyl N-(2-oxo-1-phenylethyl)carbamate

CC(C)(C)OC(=O)NC(C=O)C1=CC=CC=C1

Environmental

Product

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Previewing top 4 entries. If you want the full results, please use the download button above.

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Abiotic

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Environmental

Downstream Successor

XKXIQBVKMABYQJ-UHFFFAOYSA-M

tert-Butyl carbonate

C(=O)(OC(C)(C)C)[O-]

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Abiotic

Downstream Successor

FAQJJMHZNSSFSM-UHFFFAOYSA-N

Phenylglyoxylic Acid

c1cccc(c1)C(C(O)=O)=O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Environmental

Downstream Successor

FAQJJMHZNSSFSM-UHFFFAOYSA-N

Phenylglyoxylic Acid

c1cccc(c1)C(C(O)=O)=O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Abiotic

Downstream Successor

FAQJJMHZNSSFSM-UHFFFAOYSA-N

Phenylglyoxylic Acid

c1cccc(c1)C(C(O)=O)=O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Environmental

Downstream Successor

ZGUNAGUHMKGQNY-ZETCQYMHSA-N

L-Phenylglycine

C1=CC=C(C=C1)[C@@H](C(=O)O)N

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Abiotic

Downstream Successor

IWYDHOAUDWTVEP-UHFFFAOYSA-N

Mandelic Acid

C(C(c1ccccc1)O)(O)=O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Abiotic

Downstream Successor

HNZXTILLSIEXRZ-UHFFFAOYSA-N

2-(3,4-Dihydroxyphenyl)-2-oxoacetic acid

OC(=O)C(=O)C1=CC(=C(C=C1)O)O

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Abiotic

Downstream Successor

LFKDJXLFVYVEFG-UHFFFAOYSA-N

tert-Butyl carbamate

NC(=O)OC(C)(C)C

Precursor

HOBFSNNENNQQIU-SNVBAGLBSA-N

(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid

CC(C)(C)OC(=O)N[C@H](C1=CC=CC=C1)C(=O)O

Environmental

Downstream Successor

APHFQZJMZZWSNW-UHFFFAOYSA-N

C=1C(C=CC(C(C(=O)O)N)C1)=O

Previewing top 10 entries. If you want the full results, please use the download button above.

No Original Precursors

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